# Vitalitec Int'L., Inc.

- Location (FDA's records): Plymouth, MA
- FDA decisions: 1 (1998–1998): 1 510(k) clearance
- Product codes: FZP (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 3 (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
- Eisner USA, Inc.: 1 (https://510kreport.com/company/eisner-usa)
- Intramed Laboratories, Inc.: 1 (https://510kreport.com/company/intramed-laboratories)
- Edward Weck, Inc.: 1 (https://510kreport.com/company/edward-weck)
- United States Surgical, A Division of Tyco Healthc: 1 (https://510kreport.com/company/united-states-surgical-a-division-of-tyco-healthc)
- Axiom Medical, Inc.: 1 (https://510kreport.com/company/axiom-medical)

## Firms that cite its devices most
- Design Standards Corp.: 1 (https://510kreport.com/company/design-standards)
- Synovis Micro Companies Alliance A Subsidiary of Baxter Int: 1 (https://510kreport.com/company/synovis-micro-companies-alliance-a-subsidiary-of-baxter-int)
- Dannik: 1 (https://510kreport.com/company/dannik)

## Its most-cited devices
- K981645: Titanium Hemostatic Clip (1998), cited by 3

## Recent decisions
- K981645: Titanium Hemostatic Clip (Oct 13, 1998)

Source page: https://510kreport.com/company/vitalitec-int-l
