# Unoplast A/S

- Location (FDA's records): Denmark, DK
- FDA decisions: 7 (1980–1990): 7 510(k) clearances
- Product codes: KOD (1), BZB (1), BSY (1), FPD (1), GAO (1), EXR (1), KGX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 15 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Rusch Intl.: 1 (https://510kreport.com/company/rusch-intl)
- Convatec Limited: 1 (https://510kreport.com/company/convatec)

## Its most-cited devices
- K896729: Nelaton-, Female - or Tiemann Catheter (1990), cited by 2

## Recent decisions
- K896734: Feeding Tube (Dec 21, 1990)
- K896729: Nelaton-, Female - or Tiemann Catheter (Nov 5, 1990)
- K896732: Unometer 500 (Nov 2, 1990)
- K896731: Oxygen Catheters (Mar 30, 1990)
- K896730: Suction Catheter Straight/Coude (Mar 30, 1990)
- K896733: Vaccon (Feb 1, 1990)
- K802248: Disarp Original (Sep 26, 1980)

Source page: https://510kreport.com/company/unoplast-a-s