Amorchem Holdings, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Amorchem Holdings, Inc. makes
Amorchem Holdings, Inc. manufactures the AmorChem Titanium Porous Fixation Device, a medical implant designed for orthopedic fixation applications using porous titanium technology.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
AmorChem Titanium Porous Fixation Device Ref K160791
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Amorchem Holdings, Inc. have in the registry?
The registry currently lists 1 device for Amorchem Holdings, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amorchem Holdings, Inc.'s devices?
Among its 1 most recently registered device, Amorchem Holdings, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Amorchem Holdings, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Amorchem Holdings, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amorchem Holdings, Inc. in the registry?
The most recently registered devices listed for Amorchem Holdings, Inc. include AmorChem Titanium Porous Fixation Device.