# Specialities Remeex International, S.L.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 3 (2004–2006): 3 510(k) clearances
- Product codes: OTM (1), PAH (1), OTN (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 3 (1 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.: 1 (https://510kreport.com/company/ethicon)

## Firms that cite its devices most
- KARL STORZ Endoscopy-America, Inc.: 1 (https://510kreport.com/company/karl-storz-endoscopy-america)
- Mpathy Medical Devices, Ltd.: 1 (https://510kreport.com/company/mpathy-medical-devices)

## Its most-cited devices
- K033310: Remeex System for Urinary Incontinence (2004), cited by 3

## Recent decisions
- K063136: Needleless Sling (Dec 19, 2006)
- K062341: Male Remeex System (Nov 2, 2006)
- K033310: Remeex System for Urinary Incontinence (Jan 15, 2004)

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