Data / Medical devices / United States / Lymphatech
Lymphatech: FDA-registered device maker in Atlanta, GA, United States, 1 510(k) clearance
Lymphatech is registered with the FDA (registration 3031823375) in Atlanta, GA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 22, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3031823375
- Address
- 101 Nerem St Nw Ste 1000, Atlanta, GA, United States, 30313
- Owner or operator
- LymphaTech (10091084)
- Roles
- Manufacturer
- First device listed
- June 27, 2024
- Registered through
- 2026
- Brand names listed
- LymphaTech 3D Measuring System, LymphaTech Smart Tape Measure
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Camera, Surgical, Measurement | SFG | 1 | Manufacturer | accessdata.fda.gov |
| Tape, Measuring, Rulers And Calipers | FTY | 1 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| July 22, 2025 | K251255 | LymphaTech Mobile 3D Measuring Tool | SFG | Substantially Equivalent | Lymphatech, Inc. | accessdata.fda.gov |
Compare with other makers
Updated July 22, 2025. 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.