# Alliqua Biomedical, Inc.

- Location (FDA's records): Eden Prairie, MN
- FDA decisions: 2 (2016–2017): 2 510(k) clearances
- Product codes: NRB (1), FRO (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 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
- Celleration, Inc.: 1 (https://510kreport.com/company/celleration)

## Recent decisions
- K171041: SilverSeal (Aug 22, 2017)
- K162721: Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator (Dec 22, 2016)

Source page: https://510kreport.com/company/alliqua-biomedical