Holmed LLC
Also registered as Holmed Corp.
United Statesfrom the FDA registration address FDA establishment FEI 1219518
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Endoscopic Needleholder, Modification Ref K930330
Regimes: 510(k) Registry: 510(k)Christoudias Peritoneum Twin Tissue Approximator Ref K942597
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1219518
- Address
- 48 Frank Mossberg Drive., Attleboro, MA, 02703
Frequently asked questions
How many devices does HOLMED LLC have in the registry?
The registry currently lists 2 devices for HOLMED LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list HOLMED LLC's devices?
Among its 2 most recently registered devices, HOLMED LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do HOLMED LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for HOLMED LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from HOLMED LLC in the registry?
The most recently registered devices listed for HOLMED LLC include ENDOSCOPIC NEEDLEHOLDER, MODIFICATION and CHRISTOUDIAS PERITONEUM TWIN TISSUE APPROXIMATOR.