Super Source
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Super Source is a medical device manufacturer, with 8 devices listed in FDA GUDID (FDA Class I) as of 12 Nov 2026.
- Devices
- 8
Registry facts
- Registries
- FDA GUDID 8
- Device classes
- FDA Class I 8
- Identifiers
- DUNS 806786778
What Super Source makes
Super Source manufactures nitrile examination and treatment gloves that are non-powdered and non-antimicrobial, designed for medical and clinical use.
The company’s products are classified as Class I devices and are listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- DUNS number
- 806786778
Frequently asked questions
How many devices does Super Source have in the registry?
The registry currently lists 8 devices for Super Source. Devices recorded under merged duplicate company entries are counted once.
Which registries list Super Source's devices?
Among its 8 most recently registered devices, Super Source has devices listed in FDA GUDID (8 devices).
What risk classes do Super Source's devices fall under?
Among its 8 most recently registered devices, the classes recorded for Super Source's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Super Source in the registry?
The most recently registered devices listed for Super Source include Super Source GLO529BK, Super Source GLO528BK, Super Source GLO530BK and Super Source GLO525B.