Emerald Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Emerald Medical, Inc. makes
Emerald Medical, Inc. manufactures sterile gauze sponges, powdered and powder-free vinyl examination gloves, and a nucleus pulposis evacuator system.
The company is based in the United States and maintains device listings for Class I, Class II, and unclassified products within the FDA 510(k) regulatory registry.
Catalogue
Emerald Sterile Gauze Sponge Ref K961581
Regimes: 510(k) Registry: 510(k)Syntheticare Powdered Vinyl Examination Gloves Ref K030484
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Emerald Medical, Inc. have in the registry?
The registry currently lists 4 devices for Emerald Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Emerald Medical, Inc.'s devices?
Among its 4 most recently registered devices, Emerald Medical, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Emerald Medical, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Emerald Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Emerald Medical, Inc. in the registry?
The most recently registered devices listed for Emerald Medical, Inc. include EMERALD STERILE GAUZE SPONGE, SYNTHETICARE POWDERED VINYL EXAMINATION GLOVES, EMERALD MEDICAL, INC. NUCLEUS PULPOSIS EVACUATOR SYSTEM and SYNTHETICARE POWDER-FREE VINYL EXAMINATION GLOVES.