Data / Medical devices / United States / Stimlabs, LLC
Stimlabs, LLC: FDA-registered device maker in Roswell, GA, United States, 5 510(k) clearances
Stimlabs, LLC is registered with the FDA (registration 3012823434) in Roswell, GA, United States. It lists 1 device type. The FDA files 5 510(k) clearances under its listings, the newest dated March 19, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012823434
- Address
- 1225 Northmeadow Parkway Suite 104, Roswell, GA, United States, 30076
- Owner or operator
- StimLabs, LLC (10091057)
- Roles
- Complaint file establishment, Manufacturer, Repackager or relabeler
- First device listed
- June 24, 2024
- Registered through
- 2026
- Brand names listed
- Allacor P 1 cc, Allacor P 2 cc, Allacor P 4 cc, Architect Fx, Corplex P 1 cc, Corplex P 2 cc, Corplex P 4 cc, Derma-Gide(TM) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wound Dressing With Animal-Derived Material(S) | KGN | U | Complaint file establishment, Manufacturer, Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| March 19, 2026 | K260532 | Derma-Gide | KGN | Substantially Equivalent | Geistlich Pharma AG | accessdata.fda.gov |
| January 22, 2026 | K251323 | Device 104 Particulate | KGN | Substantially Equivalent | Geistlich Pharma AG | accessdata.fda.gov |
| February 2, 2024 | K231325 | Corplex P / Theracor P / Allacor P | KGN | Substantially Equivalent | Stimlabs, LLC | accessdata.fda.gov |
| November 8, 2018 | K182838 | Geistlich Derma-Gide | KGN | Substantially Equivalent | Geistlich Pharma AG | accessdata.fda.gov |
| February 26, 2013 | K122502 | BRIDGE EXTRACELLULAR COLLEGEN MATRIX | KGN | Substantially Equivalent | Harbor Medtech, Inc. | accessdata.fda.gov |
Compare with other makers
Updated March 19, 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.