Qfix
Active in EUDAMEDUnited Statesfrom SRN EUDAMED SRN US-MF-000002762
Qfix is a medical device manufacturer based in the United States, with 1,484 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I; EU Class I) as of 12 Nov 2026.
- Devices
- 1,484
- Registrations
- EUDAMED
Registry facts
- Registries
- FDA GUDID 1,464
- EUDAMED 397
- FDA 510(k) 7
- Device classes
- FDA Class II 1,347
- FDA Class I 107
- EU Class I 30
- Top EMDN categories
- Identifiers
- EUDAMED SRN US-MF-000002762
- DUNS 808875397
At a glance
Market reach
- European Union
- EUDAMED actor
Catalogue
Search and filter all 1,484 devicesShowing 1-50 of 1,484
Company details
- EUDAMED SRN
- US-MF-000002762
- DUNS number
- 808875397
- EUDAMED status
- Active
- EUDAMED registered name
- Qfix
- Registered address
- 440 Church Road, 19311, Avondale, Pennsylvania, United States
- regulatory@qfix.com
- Phone
- 6102680585
- PRRC contact
- Christine Eastburn
Frequently asked questions
How many devices does Qfix have in the registry?
The registry currently lists 1484 devices for Qfix. Devices recorded under merged duplicate company entries are counted once.
Which registries list Qfix's devices?
Among its 50 most recently registered devices, Qfix has devices listed in EUDAMED (36 devices) and FDA GUDID (37 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Qfix's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Qfix's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Qfix in the registry?
The most recently registered devices listed for Qfix include MTAPUID1832SG, MTAPU1.6, MTAPUID1832 and MTAPU14.