Perimed, Inc.
Country not established FDA
Perimed, Inc. is a medical device manufacturer, with 53 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II) as of 12 Nov 2026.
- Devices
- 53
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 43
- EUDAMED 21
- FDA 510(k) 10
- Device classes
- FDA Class II 44
At a glance
Market reach
- United States
- FDA establishment
Catalogue
Search and filter all 53 devicesShowing 1-50 of 53
FDA establishments
- Perimed Ab JARFALLA Stockholm · SE FEI 3003244961
Frequently asked questions
How many devices does Perimed, Inc. have in the registry?
The registry currently lists 53 devices for Perimed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Perimed, Inc.'s devices?
Among its 50 most recently registered devices, Perimed, Inc. has devices listed in EUDAMED (21 devices), FDA 510(k) (7 devices) and FDA GUDID (43 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Perimed, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Perimed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Perimed, Inc. in the registry?
The most recently registered devices listed for Perimed, Inc. include PF 6051-M Pressure Accessory Kit Metal Bayonet, PF 6040 tcpO2/pCO2 Unit, TC 550 Fixation Ring for tcpO2/CO2 and PF 6051 Pressure Accessory Kit.
Which FDA establishments are linked to Perimed, Inc.?
1 FDA establishment is linked to Perimed, Inc. in the registry; they are listed on the company page.