Etex Corp.
United StatesFDA applicant, unverified FDA FEI 3000206397
Etex Corp. is a medical device manufacturer, with 48 devices listed in FDA 510(k) and FDA GUDID (FDA Class II and I) as of 13 Nov 2026.
- Devices
- 48
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA 510(k) 25
- FDA GUDID 23
- Device classes
- FDA Class II 47
- FDA Class I 1
- Identifiers
- FDA FEI 3000206397
At a glance
Market reach
- United States
- FDA FEI
What Etex Corp. makes
Etex Corp. manufactures synthetic bone graft products, cadaveric-donor/synthetic mineral bone grafts, and bone graft delivery kits. Specific devices in their portfolio include EquivaBone®, N-Force Blue™, Flow-FX2, Gamma-bsm®, and CarriGen®.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries.
Catalogue
Search and filter all 48 devicesCompany details
- FDA FEI number
- 3000206397
- Address
- 55 Messina Dr, Braintree, MA, 02184
Frequently asked questions
How many devices does Etex Corp. have in the registry?
The registry currently lists 48 devices for Etex Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Etex Corp.'s devices?
Among its 48 most recently registered devices, Etex Corp. has devices listed in FDA 510(k) (25 devices) and FDA GUDID (23 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Etex Corp.'s devices fall under?
Among its 48 most recently registered devices, the classes recorded for Etex Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Etex Corp. in the registry?
The most recently registered devices listed for Etex Corp. include EquivaBone ® 76-6027, N-Force Blue ™ IN050-7, Flow-FX2 71-0025 and EquivaBone ® 76-6041.