# Beere Precision Medical Instruments, Kmedic, Telef

- Location (FDA's records): Kenosha, WI
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: GAT (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 10 (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
- Teleflex Medical: 1 (https://510kreport.com/company/teleflex-medical)

## Firms that cite its devices most
- Cayenne Medical, Inc.: 4 (https://510kreport.com/company/cayenne-medical)
- Teleflex Medical: 3 (https://510kreport.com/company/teleflex-medical)
- Teleflexmedical, Inc.: 1 (https://510kreport.com/company/teleflexmedical)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)

## Its most-cited devices
- K092533: Force Fiber Blue Ultra High Molecular Weight Polyethylene Non Absorbable Sutures (2009), cited by 10

## Recent decisions
- K092533: Force Fiber Blue Ultra High Molecular Weight Polyethylene Non Absorbable Sutures (Sep 15, 2009)

Source page: https://510kreport.com/company/beere-precision-medical-instruments-kmedic-telef