Solmetex, LLC
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000040024 FEI 3003040760
Solmetex, LLC is a medical device manufacturer based in the United States, with 11 devices listed in EUDAMED and FDA GUDID (FDA Class I) as of 15 Nov 2026.
- Devices
- 11
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- EUDAMED 11
- FDA GUDID 11
- Device classes
- FDA Class I 11
- Identifiers
- EUDAMED SRN US-MF-000040024
- FDA FEI 3003040760
- DUNS 958831349
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Search and filter all 11 devicesCompany details
- EUDAMED SRN
- US-MF-000040024
- FDA FEI number
- 3003040760
- DUNS number
- 958831349
- EUDAMED status
- Active
- EUDAMED registered name
- Solmetex, LLC
- Registered address
- 30, Bearfoot Rd., 01532, Northborough, United States
- quality@solmetex.com
- Phone
- 1-800-216-5505
- PRRC contact
- Roger Kampf
Frequently asked questions
How many devices does Solmetex, LLC have in the registry?
The registry currently lists 11 devices for Solmetex, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Solmetex, LLC's devices?
Among its 11 most recently registered devices, Solmetex, LLC has devices listed in EUDAMED (11 devices) and FDA GUDID (11 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Solmetex, LLC's devices fall under?
Among its 11 most recently registered devices, the classes recorded for Solmetex, LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Solmetex, LLC in the registry?
The most recently registered devices listed for Solmetex, LLC include DryShield BMD DS-SUL-600, DryShield BMD DS-MPL-005, DryShield BMD DS-SYS-002 and DryShield BMD DS-SUS-400.