Abyrx, Inc.
United Statesfrom the FDA registration address FDA FEI 3005972619
Abyrx, Inc. is a medical device manufacturer, with 35 devices listed in FDA GUDID (FDA Unclassified and Class II) as of 14 Nov 2026.
- Devices
- 35
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 35
- Device classes
- FDA Unclassified 24
- FDA Class II 8
- Identifiers
- FDA FEI 3005972619
- DUNS 078818942
At a glance
Market reach
- United States
- FDA FEI
What Abyrx, Inc. makes
ABYRX, Inc. manufactures synthetic bone wax, bone graft substitutes, and synthetic bone matrix implants, including both flowable and putty formulations for orthopaedic applications. Their portfolio includes orthopaedic cement—both non-antimicrobial and dispensable forms—and tools like curettes and spatulas designed for surgical use. Products include settable pastes, syringes, and specialized tips for precise delivery in bone repair procedures.
The company’s devices are classified under FDA’s Class II and Unclassified (U) categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Their products are regulated under U.S. medical device laws, with compliance requirements varying by classification. The manufacturer operates from the United States.
Catalogue
Search and filter all 35 devicesCompany details
- FDA FEI number
- 3005972619
- DUNS number
- 078818942
- Address
- 700 Fairfield Avenue, Stamford, CT, 06902
Frequently asked questions
How many devices does ABYRX, INC. have in the registry?
The registry currently lists 35 devices for ABYRX, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ABYRX, INC.'s devices?
Among its 35 most recently registered devices, ABYRX, INC. has devices listed in FDA GUDID (35 devices).
What risk classes do ABYRX, INC.'s devices fall under?
Among its 35 most recently registered devices, the classes recorded for ABYRX, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ABYRX, INC. in the registry?
The most recently registered devices listed for ABYRX, INC. include Montage Flowable Settable Bone Paste MON-BVF-1501FL, AHBP Press HBP-4010, Montage Settable Bone Putty MON-BVF-1604 and Hemasorb 2.0 gram OS-201NS.