Plymouth Medical
United Statesfrom the FDA registration address FDA establishment FEI 3028002947
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3028002947
- Address
- 135 Plymouth St # 310, Brooklyn, NY, 11201
Frequently asked questions
How many devices does PLYMOUTH MEDICAL have in the registry?
The registry currently lists 5 devices for PLYMOUTH MEDICAL. Devices recorded under merged duplicate company entries are counted once.
Which registries list PLYMOUTH MEDICAL's devices?
Among its 5 most recently registered devices, PLYMOUTH MEDICAL has devices listed in FDA GUDID (5 devices).
What are the newest devices from PLYMOUTH MEDICAL in the registry?
The most recently registered devices listed for PLYMOUTH MEDICAL include ExoCube EXO60ACD, ExoCube PRP60ACD, BD BDConv-Kit-ACD and ExoCube PRP120ACD.