# Reprise Biomedical, Inc.

- Location (FDA's records): Plymouth, MN
- FDA decisions: 5 (2022–2024): 5 510(k) clearances
- Names in FDA's records: Reprise Biomedical, Inc. (4); Reprise Biomedical (1)
- Product codes: KGN (5)
- 510(k) review time since 2016: median 31 days, against 194 for FDA's reviews in the same codes and years (4 of 5 faster)
- Predicates its devices cite: 5 (4 its own); citations of its devices by later devices: 4 (4 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
- Miromatrix Medical, Inc.: 1 (https://510kreport.com/company/miromatrix-medical)

## Its most-cited devices
- K223257: Miro3D Wound Matrix (2022), cited by 3
- K221520: Miro3D Wound Matrix (2022), cited by 1

## Recent decisions
- K240753: Miro3D Fibers Wound Matrix (Apr 19, 2024)
- K240277: MiroDry Wound Matrix (Mar 1, 2024)
- K231614: MiroTract Wound Matrix (Dec 13, 2023)
- K223257: Miro3D Wound Matrix (Nov 21, 2022)
- K221520: Miro3D Wound Matrix (Aug 18, 2022)

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