Remex Medical Corp.
TaiwanFDA 510(k) applicant, unverified FDA FEI 3017823294
- Devices
- 18
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Remex Medical Corp. makes
Remex Medical Corp. manufactures spinal surgery navigation systems, including standalone and combined platforms like the Remex Spine Surgery Navigation System II and the Anatase Spine Surgery Navigation System. Their portfolio also includes disposable instruments and reusable navigation tools designed for intraoperative spinal procedures.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) database. Remex Medical Corp. is based in the United States.
Catalogue
Search and filter all 18 devicesCompany details
- FDA FEI number
- 3017823294
- DUNS number
- 658198980
- Address
- 4F., No. 9, Jingke Road, Nantun Dist., Taichung
- [email protected]
- Phone
- (561) 277-9480
Frequently asked questions
How many devices does Remex Medical Corp. have in the registry?
The registry currently lists 18 devices for Remex Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Remex Medical Corp.'s devices?
Among its 18 most recently registered devices, Remex Medical Corp. has devices listed in FDA 510(k) (7 devices) and FDA GUDID (11 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Remex Medical Corp.'s devices fall under?
Among its 18 most recently registered devices, the classes recorded for Remex Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Remex Medical Corp. in the registry?
The most recently registered devices listed for Remex Medical Corp. include WatchTower INS-NEEDLE, WatchTower INS-CBLOCK, WatchTower INS-NVGHDL-A and WatchTower INS-NVGHDL-B.