Hi-Tec Implants
IsraelFDA applicant, unverified FDA
- Devices
- 939
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Hi-Tec Implants makes
Hi-Tec Implants manufactures dental implant components, including permanent and temporary preformed suprastructures, two-piece screw endosteal implants, and dental implant systems. Their portfolio also covers surgical procedure kits, abutment screws, intraoral-scanning abutment analogs, and dental implant analogs. Surgical instrumentation is provided for implant placement and restoration procedures.
All listed devices fall under FDA Class II regulation and are recorded in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.
Catalogue
Search and filter all 939 devicesShowing 1-50 of 939
FDA establishments
- Hi Tec Implants, Ltd. HERZLIA Tel Aviv · IL FEI 3004471724
Frequently asked questions
How many devices does Hi-Tec Implants have in the registry?
The registry currently lists 939 devices for Hi-Tec Implants. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hi-Tec Implants's devices?
Among its 50 most recently registered devices, Hi-Tec Implants has devices listed in FDA GUDID (50 devices).
What risk classes do Hi-Tec Implants's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Hi-Tec Implants's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hi-Tec Implants in the registry?
The most recently registered devices listed for Hi-Tec Implants include TITE-FIT/TAPERED TITE-FIT T-ZTA, SURGICAL INSTRUMENTATION SL-LIT-S, SURGICAL INSTRUMENTATION T-LOT and SURGICAL INSTRUMENTATION SHT-S.
Which FDA establishments are linked to Hi-Tec Implants?
1 FDA establishment is linked to Hi-Tec Implants in the registry; they are listed on the company page.