Pavmed, Inc.
United Statesfrom the FDA registration address FDA FEI 3017202975
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
CarpX Ref K200559
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3017202975
- DUNS number
- 079825991
- Address
- 200 Foxborough Boulevard, Foxborough, MA, 02035
- [email protected]
- Phone
- 212-949-4319
Frequently asked questions
How many devices does Pavmed, Inc. have in the registry?
The registry currently lists 2 devices for Pavmed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pavmed, Inc.'s devices?
Among its 2 most recently registered devices, Pavmed, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Pavmed, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pavmed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pavmed, Inc. in the registry?
The most recently registered devices listed for Pavmed, Inc. include CarpX 260-03506 and CarpX.