Syntermed, Inc.
Active in EUDAMEDAlso registered as Syntermed
United Statesfrom SRN EUDAMED FDA SRN US-MF-000012286 FEI 3003079232
- Devices
- 16
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Search and filter all 16 devicesCompany details
- EUDAMED SRN
- US-MF-000012286
- FDA FEI number
- 3003079232
- EUDAMED status
- Active
- EUDAMED registered name
- Syntermed, Inc.
- Registered address
- 245, S Owens Drive, 92808, Anaheim, United States
- Website
- www.syntermed.com
- [email protected]
- Phone
- 18882634446 ext 2
- PRRC contact
- Kenneth Van Train
Frequently asked questions
How many devices does Syntermed, Inc. have in the registry?
The registry currently lists 16 devices for Syntermed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Syntermed, Inc.'s devices?
Among its 16 most recently registered devices, Syntermed, Inc. has devices listed in EUDAMED (2 devices) and FDA 510(k) (14 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Syntermed, Inc.'s devices fall under?
Among its 16 most recently registered devices, the classes recorded for Syntermed, Inc.'s devices are Class IIa and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Syntermed, Inc. in the registry?
The most recently registered devices listed for Syntermed, Inc. include NeuroQ, Cardiac Toolbox, BP-SPECT V1.O and EMORY CARDIAC TOOLBOX VERSION 2.6.