# Cook Biotech Incorprated

- Location (FDA's records): West Lafayette, IN
- FDA decisions: 4 (2013–2015): 4 510(k) clearances
- Product codes: KHJ (2), FTM (2)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 1 (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
- Xomed, Inc.: 2 (https://510kreport.com/company/xomed)
- Cook Biotech, Inc.: 2 (https://510kreport.com/company/cook-biotech)
- Tei Biosciences, Inc.: 1 (https://510kreport.com/company/tei-biosciences)
- Medtronic Xomed, Inc.: 1 (https://510kreport.com/company/medtronic-xomed)

## Firms that cite its devices most
- Cook Biotech, Inc.: 1 (https://510kreport.com/company/cook-biotech)

## Its most-cited devices
- K150594: Biodesign Otologic Repair Graft (2015), cited by 1

## Recent decisions
- K150668: Biodesign Enterocutaneous Fistula Plug (Dec 9, 2015)
- K142887: SIS Inguinal Hernia Repair Graft (Oct 1, 2015)
- K150594: Biodesign Otologic Repair Graft (Sep 16, 2015)
- K121360: Biodesign Ent Repair Graft (Feb 27, 2013)

Source page: https://510kreport.com/company/cook-biotech-incorprated