# Stimlabs, LLC

- Location (FDA's records): Roswell, GA
- FDA decisions: 3 (2024–2025): 3 510(k) clearances
- Product codes: KGN (3)
- 510(k) review time since 2016: median 83 days, against 83 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Aroa Biosurgery, Ltd.: 1 (https://510kreport.com/company/aroa-biosurgery)

## Firms that cite its devices most
- BioTissue Holdings, Inc.: 1 (https://510kreport.com/company/biotissue-holdings)

## Its most-cited devices
- K231325: Corplex P / Theracor P / Allacor P (2024), cited by 3

## Recent decisions
- K253339: Theracor (Dec 22, 2025)
- K242828: Corplex P/ Theracor P/ Allacor P (Oct 18, 2024)
- K231325: Corplex P / Theracor P / Allacor P (Feb 2, 2024)

Source page: https://510kreport.com/company/stimlabs