US Medical Glove Company
United Statesfrom the FDA registration address FDA establishment FEI 3021827562
- Devices
- 9
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Nitrile Exam Gloves (Chemotherapy Drug Tested) Ref K223748
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3021827562
- Address
- 2001 N. Division ST, Harvard, IL, 60033
Frequently asked questions
How many devices does US MEDICAL GLOVE COMPANY have in the registry?
The registry currently lists 9 devices for US MEDICAL GLOVE COMPANY. Devices recorded under merged duplicate company entries are counted once.
Which registries list US MEDICAL GLOVE COMPANY's devices?
Among its 9 most recently registered devices, US MEDICAL GLOVE COMPANY has devices listed in FDA 510(k) (1 device) and FDA GUDID (8 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do US MEDICAL GLOVE COMPANY's devices fall under?
Among its 9 most recently registered devices, the classes recorded for US MEDICAL GLOVE COMPANY's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from US MEDICAL GLOVE COMPANY in the registry?
The most recently registered devices listed for US MEDICAL GLOVE COMPANY include US Medical Glove Blue Medium, US Medical Glove Blue Extra Large, US Medical Glove Blue Small and US Medical Glove Blue Large.