Anchor Implants, Ltd.
CanadaFDA applicant, unverified
- Devices
- 2
What Anchor Implants, Ltd. makes
Anchor Implants, Ltd. manufactures two-stage dental implants for osseointegration, including titanium alloy implants (e.g., ANCHOR IIA) and hydroxyapatite-coated implants (e.g., ADI/B series) designed for dental reconstruction. These devices are intended for surgical placement in the jawbone to support prosthetic teeth or restorations.
The company’s portfolio consists of Class II medical devices, regulated under the FDA’s 510(k) clearance pathway. These implants are listed in the FDA’s 510(k) registry, reflecting their compliance with U.S. regulatory requirements for dental osseointegration devices. The company is headquartered in the United States.
Catalogue
Anchor Iia/2 Stage Osseo. Tit. 6/4 Alloy Implant Ref K871887
Regimes: 510(k) Registry: 510(k)Adi/B/*/Ha-2 Stage Osseo. Hydro. Dental Implant Ref K873939
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Anchor Implants, Ltd. have in the registry?
The registry currently lists 2 devices for Anchor Implants, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anchor Implants, Ltd.'s devices?
Among its 2 most recently registered devices, Anchor Implants, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Anchor Implants, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Anchor Implants, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Anchor Implants, Ltd. in the registry?
The most recently registered devices listed for Anchor Implants, Ltd. include ANCHOR IIA/2 STAGE OSSEO. TIT. 6/4 ALLOY IMPLANT and ADI/B/*/HA-2 STAGE OSSEO. HYDRO. DENTAL IMPLANT.