Gm Dos Reis Industria E Comerico Ltda.
BrazilFDA applicant, unverified
- Devices
- 3
Catalogue
Pedimax II - Pedicular Screw Spinal System Ref K180626
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gm Dos Reis Industria E Comerico Ltda. have in the registry?
The registry currently lists 3 devices for Gm Dos Reis Industria E Comerico Ltda.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gm Dos Reis Industria E Comerico Ltda.'s devices?
Among its 3 most recently registered devices, Gm Dos Reis Industria E Comerico Ltda. has devices listed in FDA 510(k) (3 devices).
What risk classes do Gm Dos Reis Industria E Comerico Ltda.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Gm Dos Reis Industria E Comerico Ltda.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gm Dos Reis Industria E Comerico Ltda. in the registry?
The most recently registered devices listed for Gm Dos Reis Industria E Comerico Ltda. include Pedimax II - Pedicular Screw Spinal System, Mini and Micro Fragments Reconstruction System – GMReis and Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors.