Neoss, Ltd.
Country not established
Part of Neoss AB
Neoss, Ltd. is a medical device manufacturer, with 64 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 12 Nov 2026.
- Devices
- 64
Registry facts
- Registries
- FDA GUDID 54
- FDA 510(k) 10
- Device classes
- FDA Class II 35
- FDA Class I 29
- Sites and related companies
- Identifiers
- DUNS 216693627
What Neoss, Ltd. makes
Neoss, Ltd. manufactures dental implant components, including permanent and temporary preformed suprastructures, two-piece screw endosteal implants, and single-use or reusable dental drill bits. Their portfolio also includes reusable instrument trays, surgical screwdrivers, and non-bioabsorbable pliable-polymer membranes for dental regeneration.
The company’s devices are classified under FDA regulations as Class I or Class II and are listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
Search and filter all 64 devicesShowing 1-50 of 64
Company details
- DUNS number
- 216693627
- Phone
- 999-999-9999
Frequently asked questions
How many devices does Neoss, Ltd. have in the registry?
The registry currently lists 64 devices for Neoss, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neoss, Ltd.'s devices?
Among its 50 most recently registered devices, Neoss, Ltd. has devices listed in FDA GUDID (50 devices).
What risk classes do Neoss, Ltd.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Neoss, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neoss, Ltd. in the registry?
The most recently registered devices listed for Neoss, Ltd. include Neoss Implant System 90132, Neoss Implant System 41186, Neoss Implant System 90131 and Neoss Implant System 90113.