# Neomedic International S.L.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 3 (2011–2012): 3 510(k) clearances
- Names in FDA's records: Neomedic International S.L. (2); Neomedic International (1)
- Product codes: OTN (1), PBQ (1), OTP (1)
- Predicates its devices cite: 8 (0 its own); citations of its devices by later devices: 2 (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
- ETHICON, Inc.: 3 (https://510kreport.com/company/ethicon)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Caldera Medical, Inc.: 1 (https://510kreport.com/company/caldera-medical)
- Generic Medical Device, Inc.: 1 (https://510kreport.com/company/generic-medical-device)
- Uroplasty, Inc.: 1 (https://510kreport.com/company/uroplasty)
- American Medical Systems, Inc.: 1 (https://510kreport.com/company/american-medical-systems)

## Firms that cite its devices most
- Coloplast A/S: 1 (https://510kreport.com/company/coloplast-a-s)
- Pop Medical Solutions: 1 (https://510kreport.com/company/pop-medical-solutions)

## Its most-cited devices
- K120831: Anchorsure (2012), cited by 2

## Recent decisions
- K120831: Anchorsure (Oct 12, 2012)
- K103022: KIM (Dec 20, 2011)
- K102815: Surelift Prolapse System (Jul 7, 2011)

Source page: https://510kreport.com/company/neomedic-international