# Proxy Biomedical, Ltd.

- Location (FDA's records): Stillwater, MN
- FDA decisions: 6 (2005–2018): 6 510(k) clearances
- Product codes: FTL (5), OTO (1)
- Predicates its devices cite: 3 (3 its own); citations of its devices by later devices: 7 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Boston Scientific Corp: 2 (https://510kreport.com/company/boston-scientific)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Minnesota Medical Development, Inc.: 1 (https://510kreport.com/company/minnesota-medical-development)

## Its most-cited devices
- K060520: Vitamesh Macroporous PP Surgical Mesh (2006), cited by 3
- K051245: Polyform Synthetic Mesh (2005), cited by 2
- K172636: VitaMESH Macroporous PP Surgical Mesh (2018), cited by 1
- K050678: Motifmesh Soft Tissue Patch (2005), cited by 1

## Recent decisions
- K172636: VitaMESH Macroporous PP Surgical Mesh (Apr 30, 2018)
- K111121: Vitamesh (TM) Blue Lightweight Macroporous PP Surgical Mesh (May 13, 2011)
- K060520: Vitamesh Macroporous PP Surgical Mesh (Mar 28, 2006)
- K052100: Modification to Motifmesh Soft Tissue Patch (Aug 11, 2005)
- K051245: Polyform Synthetic Mesh (Jun 17, 2005)
- K050678: Motifmesh Soft Tissue Patch (May 20, 2005)

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