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Nobel Biocare Uas, Inc.

United StatesFDA applicant, unverified

Devices
31

What Nobel Biocare Uas, Inc. makes

The company manufactures dental implants, including single-piece titanium and hydroxyapatite-coated implants for osseointegration, as well as abutment systems for implant-supported restorations. It also produces orthodontic anchor systems, provisional dental implant systems, and specialized fixtures for zygomatic and standard Branemark implant placements. Drilling units and diamond-coated drills for surgical preparation are part of the portfolio, alongside scaled margin implant systems designed for precise dental reconstruction.

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company’s products are listed in the FDA’s 510(k) database, adhering to U.S. medical device compliance standards. The manufacturer operates from the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Nobel Biocare Uas, Inc. have in the registry?

The registry currently lists 31 devices for Nobel Biocare Uas, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Nobel Biocare Uas, Inc.'s devices?

Among its 31 most recently registered devices, Nobel Biocare Uas, Inc. has devices listed in FDA 510(k) (31 devices).

What risk classes do Nobel Biocare Uas, Inc.'s devices fall under?

Among its 31 most recently registered devices, the classes recorded for Nobel Biocare Uas, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Nobel Biocare Uas, Inc. in the registry?

The most recently registered devices listed for Nobel Biocare Uas, Inc. include REPLACE ONE PIECE IMPLANT, HA, REPLACE ONE PIECE IMPLANT, TIUNITE, PROCERA PREPARABLE ABUTMENT SYSTEM, NOBEL PERFECT IMPLANT SYSTEM and REPLACE HA COATED IMPLANT, MODELS 35102, 35132, 35162, 43102, 43132, 43162, 50102, 50132, 50162, 60102, 60132, & 60162.

Generated automatically from registry data and not verified by a human reviewer.