# Epitek, Inc.

- Location (FDA's records): Bloomington, MN
- FDA decisions: 3 (2008–2008): 3 510(k) clearances
- Product codes: ODC (1), GAT (1), FBO (1)
- Predicates its devices cite: 4 (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
- Usgi Medical: 1 (https://510kreport.com/company/usgi-medical)
- Genzyme Biosurgery: 1 (https://510kreport.com/company/genzyme-biosurgery)
- Sentreheart, Inc.: 1 (https://510kreport.com/company/sentreheart)
- Omnisonics Medical Technologies: 1 (https://510kreport.com/company/omnisonics-medical-technologies)

## Recent decisions
- K080780: Anchorage Scope, Model 000003 (Jul 30, 2008)
- K073507: Anchorage Access Kit (Mar 5, 2008)
- K073096: Anchorage Closure Device (Feb 7, 2008)

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