IP Library › Granted Patent US 9,782,324
Granted Patent B2
US 9,782,324 · App. 14/205,105 · Granted Oct 10, 2017

System and method for treating skin and underlying tissues for improved health, function and/or appearance

Inventors: John Crunick (Cranberry Township, PA); Tamas Becse (Wexford, PA); Louis L. Laskey, Jr. (Prospect, PA)
Assignee: Sigma Instruments Holdings, LLC
A61H23/02A61B5/05A61B5/053A61B5/0531A61H23/006A61H23/0218A61H23/0236A61H23/0245A61N1/328A61B5/0488A61H2201/10A61H2201/165A61H2201/5015A61H2201/5035A61H2201/5038A61H2201/5043A61H2201/5046A61H2201/5061A61H2201/5071A61H2201/5084A61H2205/022A61H2230/605
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Quick Facts
Patent No.
US 9,782,324
App. No.
14/205,105
Granted
Oct 10, 2017
Kind
B2
Abstract

Systems and methods for treating facial soft tissues of a patient in a healthcare or cosmetic treatment environment such as, for example, a spa, clinic, or a medical practitioner's office are presented herein. The facial treatment system includes a facial stimulator instrument and/or an acoustic oscillator to deliver therapeutic stimulation to the facial tissues of a patient including percussive massage, electrical stimulation, and acoustic stimulation. A facial treatment application executing on a processor of a computing device identifies a treatment protocol and operates the facial stimulator instrument and/or acoustic oscillator to implement the facial tissue treatment.

Claims (34)

1. A system for cosmetically treating tissue of a patient for at least one of improving skin appearance, reducing skin wrinkles, improving skin tone, or improving tissue function, the system comprising:

a display configured to display information associated with the treatment of the tissue;

an input in electrical communication with the display and including a key board and touch screen, the input configured to receive information associated with the treatment of the tissue;

a central processing unit (CPU) in electrical communication with the input;

a memory in electrical communication with the CPU and including treatment parameters associated with the treatment of the tissue;

a first radio frequency (RF) head capable of being placed in electrical communication with the CPU and comprising an array of piezoelectric transducers, the array configured to generate RF over a range of frequencies not possible via a single piezoelectric transducer; and

a RF receiver antenna capable of being placed in electrical communication with the CPU and configured to detect RF energy transmitted through the tissue from the first RF head;

a plurality of second RF heads, each second RF head having a piezoelectric transducer tuned to a unique frequency and capable of being placed in electrical communication with the CPU; and

an EMG sensor capable of being placed in electrical communication with the CPU and configured to detect electromyogram in the tissue;

wherein, when the first RF head and RF receiver antenna are applied to the tissue, the system is configured to: a) cause the first RF head to administer RF energy to the tissue over a range of RF frequencies; b) cause the RF receiver antenna to sense the administered RF energy transmitted through the tissue; c) identify which RF frequency of the range of RF frequencies administered to the tissue has the most transmissibility through the tissue; and d) recommend a second RF head of the plurality of second RF heads that is capable of providing the identified RF frequency,

wherein, when the recommended second RF head and EMG sensor are applied to the tissue, the system is configured to: a) cause the recommended second RF head to administer RF energy at the identified RF frequency to the tissue over a range of pulse frequencies; b) cause the EMG sensor to detect electromyogram in the tissue arising due to the RF energy administered to the tissue over the range of pulse frequencies; c) identify which pulse frequency of the range of pulse frequencies administered to the tissue causes the highest electromyogram readings in the tissue; and d) treat the tissue with the recommended second RF head at the identified RF frequency at the identified pulse frequency.

2. The system of claim 1 , wherein the array is configured to generate RF over a range of between 500 KHz and 1.5 MHz.

3. The system of claim 2 , wherein the array is configured to generate RF over a range of between 500 KHz and 1.5 MHz at steps of between 50 KHz and 200 KHz.

4. The system of claim 1 , where the piezoelectric transducers of the array includes a first piezoelectric transducer, a second piezoelectric transducer, and a third piezoelectric transducer, wherein each of the first, second and third piezoelectric transducers generate RF at distinct frequencies from each other.

5. The system of claim 1 , wherein the plurality of second RF heads includes individual second RF heads each tuned to a unique frequency from each other and each unique frequency is between 500 KHz and 1.5 MHz.

6. The system of claim 1 , wherein, when the recommended second RF head is caused to administer RF energy at the identified RF frequency to the patient over a range of pulse frequencies, range of pulse frequencies is between 1 Hz and 300 Hz.

7. The system of claim 6 , wherein the recommended second RF head is caused to administer RF energy at the identified RF frequency to the patient over the pulse frequency range of between 500 KHz and 1.5 MHz at steps programmatically controlled and optimized for tissue type via stored protocols.

8. The system of claim 1 , further comprising an impulse head capable of being placed in electrical communication with the CPU and including a solenoid driven anvil configured to deliver mechanical impulse energy to the tissue, the impulse head further including a transducer sensor for detecting a wave generated in the tissue via the administration of the mechanical impulse energy to the tissue.

9. The system of claim 1 , further comprising an electrode capable of being placed in electrical communication with the CPU and configured to administer electrical stimulation to the tissue and read electrical characteristics of the tissue in response to the electrical stimulation.

10. The system of claim 9 , wherein the electrode is supported on the impulse head.

11. The system of claim 1 , further comprising a camera capable of being placed in electrical communication with the CPU and configured to take images of the tissue, the system being configured to compare images of the tissue taken pre and post treatment via the system.

12. A method for cosmetically treating tissue of a patient for at least one of improving skin appearance, reducing skin wrinkles, improving skin tone, or improving tissue function, the method comprising:

administering RF energy to the tissue over a range of RF frequencies;

detecting the administered RF energy;

identifying which RF frequency of the range of RF frequencies has the greatest transmissibility through the tissue;

recommending the identified RF frequency for use in further RF energy treatment to the tissue; administering the RF energy at the identified RF frequency to the tissue over a range of pulse frequencies;

identifying which pulse frequency of the range of pulse frequencies results in the highest electromyogram readings in the tissue;

recommending the identified pulse frequency for use in further RF energy treatment to the tissue; and

administering the RF energy at the identified RF frequency and identified pulse frequency to the tissue.

13. The method of claim 12 , wherein the administration of the RF energy to the tissue over the range of frequencies is accomplished via a RF head having an array of piezoelectric transducers each tuned to an individual unique frequency, the array being configured to generate RF over a range of between 500 KHz and 1.5 MHz.

14. The method of claim 12 , wherein the administration of the RF energy to the tissue over the range of frequencies is over a range of between 500 KHz and 1.5 MHz at steps of between 50 KHz and 200 KHz.

15. The method of claim 12 , wherein the recommending the identified RF frequency for use in further RF energy treatment to the tissue includes identifying a specific RF head from a plurality of RF heads that is configured to provide the recommended RF frequency.

16. The method of claim 12 , wherein the administering the RF energy at the identified RF frequency to the tissue over a range of pulse frequencies occurs over a pulse frequencies ranging between 1 Hz and 300 Hz programmatically controlled and optimized for tissue type via stored protocols.

17. The method of claim 12 , wherein the administering the RF energy at the identified RF frequency to the patient over a range of pulse frequencies occurs over a pulse frequencies ranging between 1 Hz and 30 Hz.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 11, 2014
From: CRUNICK, JOHN; BECSE, TAMAS; LASKEY, LOUIS L., JR.
To: SIGMA INSTRUMENTS HOLDINGS, LLC
Reel/Frame 032409/0013 →
Continuity (5)
Continuation In Part PCTUS2012055551 · Sep 14, 2012
Provisional Application 61616967 · Mar 28, 2012
Provisional Application 61535225 · Sep 15, 2011
Provisional Application 61791203 · Mar 15, 2013
Related Publication 20140194790A1 · Jul 10, 2014