Romear Mfg., Inc.
Country not established
- Devices
- 1
What Romear Mfg., Inc. makes
Romear Mfg., Inc. manufactures the PERSONAL ROMEAR, a Class I medical device designed for personal use.
The device is regulated under FDA 510(k) clearance and is listed in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Personal Romear Ref K823588
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Romear Mfg., Inc. have in the registry?
The registry currently lists 1 device for Romear Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Romear Mfg., Inc.'s devices?
Among its 1 most recently registered device, Romear Mfg., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Romear Mfg., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Romear Mfg., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Romear Mfg., Inc. in the registry?
The most recently registered devices listed for Romear Mfg., Inc. include PERSONAL ROMEAR.