Remex Medical Corp.

FDA Regulatory Profile

Remex Medical Corp. has 0 FDA recalls, 0 inspections, 7 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Aug 20, 2026

Reviewing Remex Medical Corp. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Request a free FDA snapshot

Or get Remex Medical Corp.'s full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site, in Claude, Cursor or ChatGPT.

Get a free API key

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances7Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K262506Remex Spine Surgery Navigation - Universal InstrumentsAug 20, 2026
K251315Anatase Spine Surgery Navigation System and Remex Spine Surgery Navigation System IIMay 29, 2025
K243560Remex Spine Surgery Navigation InstrumentDec 13, 2024
K241625Anatase Navi Disposable InstrumentJul 5, 2024
K233513Remex Spine Surgery Navigation System IIMay 1, 2024
K230783Anatase Spine Surgery Navigation SystemApr 21, 2023
K220348Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-VJul 14, 2022