Nobelpharma USA, Inc.
United StatesFDA applicant, unverified
- Devices
- 64
What Nobelpharma USA, Inc. makes
Nobelpharma USA, Inc. manufactures dental implant components, including angulated and single-tooth abutments, healing abutments, and fixture systems in titanium and gold. Their portfolio also covers attachment systems like ball attachments, guide pins, and esthetic abutments designed for dental prosthetics. Additional items include healing caps and cylinders for osseointegration support during implant recovery.
The company’s devices are regulated under FDA 510(k) clearance, with most classified as Class I or Class II. Products are listed in the FDA’s 510(k) registry, reflecting their compliance with U.S. medical device regulations. The manufacturer operates from the United States.
Catalogue
Search and filter all 64 devicesShowing 1-50 of 64
Frequently asked questions
How many devices does Nobelpharma USA, Inc. have in the registry?
The registry currently lists 64 devices for Nobelpharma USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nobelpharma USA, Inc.'s devices?
Among its 50 most recently registered devices, Nobelpharma USA, Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do Nobelpharma USA, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Nobelpharma USA, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nobelpharma USA, Inc. in the registry?
The most recently registered devices listed for Nobelpharma USA, Inc. include BRANEMARK SYSTEM 17 ANGULATED ABUTMENT, BRANEMARK SYSTEM, BRANEMARK SYSTEM ESTHETICONE ABUTMENT COMPLETE and BRANEMARK SYSTEM-3.0MM FIXTURE.