# Remex Medical Corp.

- Location (FDA's records): Taichung, TW
- FDA decisions: 7 (2022–2026): 7 510(k) clearances
- Names in FDA's records: Remex Medical Corp. (6); Remex Medical Corporation (1)
- Product codes: OLO (7)
- 510(k) review time since 2016: median 30 days, against 90 for FDA's reviews in the same codes and years (5 of 7 faster)
- Predicates its devices cite: 13 (9 its own); citations of its devices by later devices: 9 (9 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
- Intai Technology Corporation: 4 (https://510kreport.com/company/intai-technology)

## Its most-cited devices
- K233513: Remex Spine Surgery Navigation System II (2024), cited by 3
- K220348: Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V (2022), cited by 3
- K230783: Anatase Spine Surgery Navigation System (2023), cited by 2
- K251315: Anatase Spine Surgery Navigation System and Remex Spine Surgery Navigation System II (2025), cited by 1

## Recent decisions
- K262506: Remex Spine Surgery Navigation - Universal Instruments (Aug 20, 2026)
- K251315: Anatase Spine Surgery Navigation System and Remex Spine Surgery Navigation System II (May 29, 2025)
- K243560: Remex Spine Surgery Navigation Instrument (Dec 13, 2024)
- K241625: Anatase Navi Disposable Instrument (Jul 5, 2024)
- K233513: Remex Spine Surgery Navigation System II (May 1, 2024)
- K230783: Anatase Spine Surgery Navigation System (Apr 21, 2023)
- K220348: Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V (Jul 14, 2022)

Source page: https://510kreport.com/company/remex-medical