Temrex Corp.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000018366 FEI 2429849
Temrex Corp. is a medical device manufacturer based in the United States, with 58 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I; EU Class I) as of 13 Nov 2026.
- Devices
- 58
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 53
- EUDAMED 14
- FDA 510(k) 2
- Device classes
- FDA Class II 42
- FDA Class I 13
- EU Class I 3
- Top EMDN categories
- Identifiers
- EUDAMED SRN US-MF-000018366
- FDA FEI 2429849
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Search and filter all 58 devicesShowing 1-50 of 58
Company details
- EUDAMED SRN
- US-MF-000018366
- FDA FEI number
- 2429849
- EUDAMED status
- Active
- EUDAMED registered name
- Temrex Corporation
- EUDAMED abbreviated name
- Temrex
- Registered address
- 300 BUFFALO AVE., 11520, Freeport, United States
- Website
- www.temrex.com
- Phone
- +001 15168686221
- PRRC contact
- andrew shapiro
Frequently asked questions
How many devices does Temrex Corp. have in the registry?
The registry currently lists 58 devices for Temrex Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Temrex Corp.'s devices?
Among its 50 most recently registered devices, Temrex Corp. has devices listed in EUDAMED (12 devices) and FDA GUDID (47 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Temrex Corp.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Temrex Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Temrex Corp. in the registry?
The most recently registered devices listed for Temrex Corp. include TEMREX, Temrex Cement, COPALITE 4002 and INTERVAL 7500.