Mid-America Safety Corp
United Statesfrom the FDA registration address FDA establishment FEI 3018382937
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
MASC Surgical Mask Ref K211984
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3018382937
- Address
- 800 Greenleaf Ave, Elk Grove Village, IL, 60007
Frequently asked questions
How many devices does MID-AMERICA SAFETY CORP have in the registry?
The registry currently lists 3 devices for MID-AMERICA SAFETY CORP. Devices recorded under merged duplicate company entries are counted once.
Which registries list MID-AMERICA SAFETY CORP's devices?
Among its 3 most recently registered devices, MID-AMERICA SAFETY CORP has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do MID-AMERICA SAFETY CORP's devices fall under?
Among its 3 most recently registered devices, the classes recorded for MID-AMERICA SAFETY CORP's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from MID-AMERICA SAFETY CORP in the registry?
The most recently registered devices listed for MID-AMERICA SAFETY CORP include MASC 860006984205, MASC 860006984267 and MASC Surgical Mask.