Data / Medical devices / United States / Technological Medical Advancements, LLC
Technological Medical Advancements, LLC: FDA-registered device maker in West Palm Bch, FL, United States, 1 510(k) clearance
Technological Medical Advancements, LLC is registered with the FDA (registration 3009346095) in West Palm Bch, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 23, 2012. 1 recall event names it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009346095
- Address
- 245 Greymon Dr, West Palm Bch, FL, United States, 33405
- Owner or operator
- Technological Medical Advancements, LLC (10043436)
- Roles
- Specification developer
- First device listed
- February 15, 2013
- Registered through
- 2026
- Brand names listed
- Diowave 100 WLS, Diowave 250WLS, Diowave Stealth Lite DSL, Diowave Stealth Max DSM
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 23, 2012 | K121363 | DIOWAVE LOW LEVEL COLD LASER SYSTEM | ILY | Substantially Equivalent | Technological Medical Advancments, Inc. (Tma) | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| January 9, 2026 | 98507 | Class II | Ongoing | Diowave Laser System, REF: Diowave 250W | Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness associated with minor arthritis, and to temporarily increase local blood circulation, operating at a maximum average power output of 70W, which is beyond the FDA cleared 60W. | accessdata.fda.gov |
Compare with other makers
Updated May 11, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.