MarketHATCH Co. Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3009410372
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3009410372
- Address
- 91 E Voris St, Akron, OH, 44311
Frequently asked questions
How many devices does MarketHATCH Co. Inc. have in the registry?
The registry currently lists 4 devices for MarketHATCH Co. Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MarketHATCH Co. Inc.'s devices?
Among its 4 most recently registered devices, MarketHATCH Co. Inc. has devices listed in FDA GUDID (4 devices).
What risk classes do MarketHATCH Co. Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for MarketHATCH Co. Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from MarketHATCH Co. Inc. in the registry?
The most recently registered devices listed for MarketHATCH Co. Inc. include Tape PlasTape, Tape PapeTapeLong, Tape PlasTapeLong and Tape PapeTape.