IP Library Granted Patent US 12,611,545
Granted Patent B2
US 12,611,545 · App. 18/363,478 · Granted Apr 28, 2026

Device and method for unattended treatment of a patient

Inventors: Tomás Schwarz (Prague, CZ); Lucia Jelínková (Prague, CZ); Vojtech Kubík (Břevnov, CZ)
Assignee: BTL Healthcare Technologies A.S.
A61N2/002A61N1/403A61N2/02
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Quick Facts
Patent No.
US 12,611,545
App. No.
18/363,478
Granted
Apr 28, 2026
Kind
B2
Abstract

An unattended approach can increase the reproducibility and safety of the treatment as the chance of over/under treating of a certain area is significantly decreased. On the other hand, unattended treatment of uneven or rugged areas can be challenging in terms of maintaining proper distance or contact with the treated tissue, mostly on areas which tend to differ from patient to patient (e.g. facial area). Delivering energy via a system of active elements embedded in a flexible pad adhesively attached to the skin offers a possible solution. The unattended approach may include delivering of multiple energies to enhance a visual appearance.

Claims (91)

1 . A device for a treatment of a patient, comprising:

a first generator configured to generate a first type of energy, wherein the first type of energy is a radiofrequency energy with a frequency in a range of 100 kHz to 550 MHz;

a second generator configured to generate a second type of energy, wherein the second type of energy is a pulsed magnetic field with a pulse duration in a range of 3 μs to 1 ms;

a switching circuit;

a user interface configured to allow an operator of the device to select a treatment protocol;

a control unit configured to control the first generator, the second generator, and the switching circuit according to the treatment protocol selected by the operator; and

a flexible pad having a surface area in a range of 0.1 cm 2 to 150 cm 2 and configured to be attached to the body part during the treatment, the flexible pad comprising:

an active element having a surface area in a range of 0.1 cm 2 to 70 cm 2 and configured to:

be coupled to the first generator and the second generator via the switching circuit,

be coupled to a body part of the patient during the treatment,

provide the first type of energy to the body part to cause heating of a skin of the body part, and

provide the second type of energy to the body part to stimulate a muscle within the body part,

wherein the body part comprises a face, a neck, or a submentum, and

wherein the control unit is configured to electrically connect the active element with the first generator or the second generator via the switching circuit based on the treatment protocol.

2 . The device of claim 1 , wherein a distance between a nearest point of the active element and an edge of the flexible pad is in a range of 0.1 to 10 mm.

3 . The device of claim 2 , wherein the flexible pad is configured to be attached to the body part by an adhesive layer.

4 . The device of claim 3 , wherein the adhesive layer comprises an adhesive tape or an adhesive gel.

5 . The device of claim 3 , wherein the muscle stimulation causes a muscle contraction, and

wherein the control unit is configured to control the second type of energy to cause 60 to 900 muscle contractions per treatment.

6 . The device of claim 1 , wherein the active element comprises a coil, and

wherein the pulsed magnetic field has a magnetic flux density on a surface of the coil in a range of 0.01 T to 7 T and a repetition frequency of magnetic pulses in a range of 2 Hz to 600 Hz.

7 . The device of claim 6 , wherein the pulsed magnetic field has a maximum value of a magnetic flux density derivative in a range of 1 T/s to 800 kT/s.

8 . A device for a treatment of a patient, comprising:

a first generator configured to generate a first energy;

a second generator configured to generate a second energy different than the first energy;

a control unit configured to control the first generator and the second generator;

a pad having a surface area in a range of 0.1 cm 2 to 150 cm 2 , configured to be coupled to the first generator and the second generator and configured to be attached to a face of a patient during the treatment, the pad comprising:

a flexible substrate comprising an underside configured to face the patient during the treatment;

a first active element coupled to the underside of the flexible substrate and configured to provide the first energy to the face to cause heating of the face; and

a second active element distanced from the first active element in a range of 0.5 mm to 60 mm and configured to provide the second energy to the face to stimulate a muscle within the face,

wherein the muscle comprises frontalis muscle, procerus muscle, buccinators muscle, risorius muscle, zygomaticus muscle, or masseter muscle; and

an adhesive layer configured to attach the pad to a fixed position on the face.

9 . The device of claim 8 , wherein the first active element is flexible and has a stiffness in a range of shore OO30 to A100, and the second active element is rigid.

10 . The device of claim 8 , wherein the control unit is configured to provide the first energy and the second energy simultaneously for at least a subset of a duration of the treatment.

11 . The device of claim 10 , wherein the flexible substrate comprises a polymer-based material, a silicone-based material, or fabric.

12 . The device of claim 11 , wherein the first energy is a radiofrequency energy, and the second energy is a pulse magnetic field having a pulse duration in a range of 0.5 μs to 500 ms.

13 . The device of claim 12 , wherein the first active element is a radiofrequency electrode having a surface area in a range of 1 cm 2 to 25 cm 2 ; and

wherein the second active element is a coil embedded in the substrate.

14 . The device of claim 13 , wherein the radiofrequency electrode has a thickness in a range of 0.2 mm to 10 mm.

15 . A device for a treatment of a patient, comprising:

a main unit, comprising:

a first generator configured to generate a first type of energy;

a second generator configured to generate a second type of energy in pulses having a pulse duration in a range of 0.5 μs to 500 ms; and

a control unit configured to control the first generator and the second generator;

a first pad having a surface area in a range of 0.5 cm 2 to 100 cm 2 and configured to be attached to a left cheek of a patient during a treatment, the first pad comprising:

a first active element having a surface area in a range of 0.1 cm 2 to 70 cm 2 and configured to provide the first type of energy to the left cheek to cause heating of the left cheek;

a second pad having a surface area in a range of 0.5 cm 2 to 100 cm 2 and configured to be attached to a right cheek of the patient during the treatment, the second pad comprising:

a second active element configured to provide the second type of energy to the right cheek to stimulate a muscle within the right cheek,

wherein the second pad has a polygonal shape comprising a convex curvature and a concave curvature in a floor projection of a surface side configured to be attached to the right cheek, and

wherein the second active element is positioned in the pad to stimulate at least one of buccinators muscle, risorius muscle, zygomaticus muscle, or masseter muscle; and

an interconnecting block between the first pad and the main unit and between the second pad and the main unit, and configured to couple the first pad to the first generator and to couple the second pad to the second generator.

16 . The device of claim 15 , wherein the interconnecting block is movable relative to the main unit.

17 . The device of claim 15 , further comprising:

a first applicator, comprising:

the first pad;

a first connecting part coupled to the first pad on a first side; and

a first connector coupled to the first connecting part on a second side opposite the first side; and

a second applicator, comprising:

the second pad;

a second connecting part coupled to the second pad on a first side; and

a second connector coupled to the second connecting part on a second side opposite the first side,

wherein the interconnecting block comprises a first socket configured to connect the first connector of the first applicator and a second socket configured to connect the second connector of the second applicator.

18 . The device of claim 15 , wherein the first active element comprises a radiofrequency electrode, and the first type of energy is radiofrequency energy; and

wherein the second active element comprises a coil, and the second type of energy is a pulsed magnetic field.

19 . The device of claim 18 , wherein the pulsed magnetic field has a magnetic flux density on a surface of the coil in a range of 0.01 T to 7 T, a pulse duration in a range of 3 μs to 1 ms, and a repetition frequency of magnetic pulses in a range of 2 Hz to 600 Hz.

20 . The device of claim 19 , wherein the pulsed magnetic field has a maximum value of a magnetic flux density derivative in a range of 1 T/s to 800 kT/s, and wherein an inductance of the coil is in a range of 1 nH to 500 mH.

21 . The device of claim 18 , wherein the radiofrequency energy has an output power in a range of 1 W to 200 W and a frequency in a range of 400 kHz to 80 MHz.

22 . A device for a treatment of a patient, comprising:

a first generator configured to generate a first type of energy;

a second generator configured to generate a second type of energy;

a control unit configured to control the first generator and the second generator;

a first pad having a surface area in a range of 0.5 cm 2 to 100 cm 2 and configured to be attached to a left cheek of a patient during the treatment, the first pad comprising:

a first active element having a surface area in a range of 0.5 cm 2 to 50 cm 2 and configured to provide the first type of energy to the left cheek to cause heating of a skin of the left cheek; and

a second active element configured to provide the second type of energy to the left cheek to stimulate a muscle within the left cheek;

a second pad having a surface area in a range of 0.5 cm 2 to 100 cm 2 and configured to be attached to a right cheek of a patient during the treatment, the second pad comprising:

a third active element having a surface area in a range of 0.5 cm 2 to 50 cm 2 and configured to provide the first type of energy to the right cheek to cause heating of a skin of the right cheek; and

a fourth active element configured to provide the second type of energy to the right cheek to stimulate a muscle within the right cheek; and

an interconnecting block configured to couple the first pad to the first generator and the second generator and to couple the second pad to the first generator and the second generator,

wherein the control unit is configured to provide the first type of energy or the second type of energy via the first pad and the second pad simultaneously for at least a subset of a duration of the treatment.

23 . The device of claim 22 , further comprising a third pad having a surface area in a range of 0.2 cm 2 to 125 cm 2 and configured to be attached to a forehead of a patient during the treatment, the third pad comprising:

a fifth active element having a surface area in a range of 0.5 cm 2 to 50 cm 2 and configured to provide the first type of energy to the forehead to cause heating of a skin of the forehead; and

a sixth active element configured to provide the second type of energy to the forehead to stimulate a muscle within the forehead,

wherein the interconnecting block is configured to couple the third pad to the first generator and the second generator, and

wherein the control unit is configured to provide the first type of energy or the second type of energy via the first pad and the third pad simultaneously for at least a subset of a duration of the treatment.

24 . The device of claim 23 , wherein the first pad and the second pad are configured to be positioned such that the second active element and the fourth active element are configured to stimulate at least one of buccinators muscle, risorius muscle, zygomaticus muscle, or masseter muscle, and

wherein the third pad is configured to be positioned such that the sixth active element is configured to stimulate at least one of frontalis muscle, or procerus muscle.

25 . The device of claim 24 , wherein the first pad is flexible and further comprises a flexible substrate comprising an underside configured to face the patient during the treatment.

26 . The device of claim 25 , wherein the first active element is a radiofrequency electrode positioned on the underside of the flexible substrate, and wherein the second active element is a coil embedded in the flexible substrate.

27 . The device of claim 26 , wherein the first pad has a thickness in a range of 0.01 mm to 15 mm.

28 . The device of claim 27 , wherein the flexible substrate comprises at least one of a polymer-based material, silicone-based material, or fabric.

29 . The device of claim 28 , wherein the first pad is configured to be attached to the left cheek by a first adhesive layer, the second pad is configured to be attached to the right cheek by a second adhesive layer, and the third pad is configured to be attached to the forehead by a third adhesive layer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 24, 2025
From: SCHWARZ, TOMÁS; JELÍNKOVÁ, LUCIA; KUBÍK, VOJTECH
To: BTL HEALTHCARE TECHNOLOGIES A.S.
Reel/Frame 070301/0534 →
Continuity (8)
Continuation PCTEP2022080502 · Nov 2, 2022
Continuation In Part 17664161 · May 19, 2022
Continuation In Part 17518243 · Nov 3, 2021
Continuation In Part 17664161 · May 19, 2022
Continuation In Part 17518243 · Nov 3, 2021
Continuation In Part PCTIB2021000300 · May 3, 2021
Provisional Application 63019619 · May 4, 2020
Related Publication 20240091547A1 · Mar 21, 2024
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