# Tutogen Medical U.S., Inc.

- Location (FDA's records): Alachua, FL
- FDA decisions: 2 (2000–2008): 2 510(k) clearances
- Product codes: FTM (1), NPL (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 4 (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
- Bio-Vascular, Inc.: 1 (https://510kreport.com/company/bio-vascular)

## Firms that cite its devices most
- Collagen Matrix, Inc.: 2 (https://510kreport.com/company/collagen-matrix)
- Obi Biologics, Inc.: 1 (https://510kreport.com/company/obi-biologics)
- Kensey Nash Corp.: 1 (https://510kreport.com/company/kensey-nash)

## Its most-cited devices
- K073097: Tutodent Dental Membrane (2008), cited by 4

## Recent decisions
- K073097: Tutodent Dental Membrane (May 12, 2008)
- K991296: Tutopatch (Oct 6, 2000)

Source page: https://510kreport.com/company/tutogen-medical-us
