# Abanza Tecnomed S.L

- Location (FDA's records): Mutilva, ES
- FDA decisions: 4 (2022–2026): 4 510(k) clearances
- Product codes: MBI (4)
- 510(k) review time since 2016: median 54 days, against 61 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 6 (3 its own); citations of its devices by later devices: 3 (3 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
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Parcus Medical, LLC: 1 (https://510kreport.com/company/parcus-medical)
- OrthoPediatrics Corp.: 1 (https://510kreport.com/company/orthopediatrics)

## Its most-cited devices
- K212197: WasherCap Fixation System (2022), cited by 2
- K243712: WasherCap™ Mini Fixation System (Model 45) (2025), cited by 1

## Recent decisions
- K253618: QuadLock™ Fixation System (Jan 6, 2026)
- K250238: WasherCap™ Fixation System (Feb 25, 2025)
- K243712: WasherCap™ Mini Fixation System (Model 45) (Jan 30, 2025)
- K212197: WasherCap Fixation System (Sep 22, 2022)

Source page: https://510kreport.com/company/abanza-tecnomed-s-l