Linvatec Biomaterials, Ltd.
Country not established
- Devices
- 8
Catalogue
Modification To Smartpin Ref K041288
Regimes: 510(k) Registry: 510(k)Biosorb Fx And Biosorb Pdx 1.5 And 2.0 Screws Ref K042517
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Matryx Interference Screw Ref K052080
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Duet Suture Anchor, Models BXS4216, BXS4216H; Impact Suture Anchor, Models BXS4218, BXS4218H Ref K042966
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Linvatec Biomaterials, Ltd. have in the registry?
The registry currently lists 8 devices for Linvatec Biomaterials, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Linvatec Biomaterials, Ltd.'s devices?
Among its 8 most recently registered devices, Linvatec Biomaterials, Ltd. has devices listed in FDA 510(k) (8 devices).
What risk classes do Linvatec Biomaterials, Ltd.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Linvatec Biomaterials, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Linvatec Biomaterials, Ltd. in the registry?
The most recently registered devices listed for Linvatec Biomaterials, Ltd. include MODIFICATION TO SMARTPIN, BIOSORB FX AND BIOSORB PDX 1.5 AND 2.0 SCREWS, SMARTSCREW II, MODELS 232010, 232012, 232014, 232016, 232018, 232020 and 2.4 SMARTNAIL, MODELS 532416, 532425, 532435, 532445.