Sargon Ent., Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Sargon Ent., Inc. makes
Sargon Ent., Inc. manufactures dental implants, including the Sargon Cylindro-Blade Implant, Sargon Immediate Load Implant (Model D), and Sargon Non-Expandable Dental Implant. These devices are designed for osseointegrated fixation in oral and maxillofacial applications, supporting single-tooth or multi-tooth restoration.
The company’s portfolio is classified under FDA Class II devices and is listed via the 510(k) pathway. These implants are intended for use in the United States, where regulatory compliance is required for market authorisation.
Catalogue
Sargon Cylindro-Blade Implant Ref K930071
Regimes: 510(k) Registry: 510(k)Sargon Immediate Load Implant, Model D Ref K981141
Regimes: 510(k) Registry: 510(k)Sargon Non-Expandable Dental Implant Ref K082573
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sargon Ent., Inc. have in the registry?
The registry currently lists 3 devices for Sargon Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sargon Ent., Inc.'s devices?
Among its 3 most recently registered devices, Sargon Ent., Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Sargon Ent., Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Sargon Ent., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sargon Ent., Inc. in the registry?
The most recently registered devices listed for Sargon Ent., Inc. include SARGON CYLINDRO-BLADE IMPLANT, SARGON IMMEDIATE LOAD IMPLANT, MODEL D and SARGON NON-EXPANDABLE DENTAL IMPLANT.