Ascent Consumer Products, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3009595561
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
Saline Wound Wash, SteriCleanse(TM) Ref K183662
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3009595561
- Address
- 105 Baylis Rd, Melville, NY, 11747
Frequently asked questions
How many devices does ASCENT CONSUMER PRODUCTS, INC. have in the registry?
The registry currently lists 3 devices for ASCENT CONSUMER PRODUCTS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ASCENT CONSUMER PRODUCTS, INC.'s devices?
Among its 3 most recently registered devices, ASCENT CONSUMER PRODUCTS, INC. 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 ASCENT CONSUMER PRODUCTS, INC.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for ASCENT CONSUMER PRODUCTS, INC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from ASCENT CONSUMER PRODUCTS, INC. in the registry?
The most recently registered devices listed for ASCENT CONSUMER PRODUCTS, INC. include SINUCLEANSE NASAL DRY SALT INHALER 00-70100, SINUCLEANSE BRONCHIAL DRY SALT INHALER 00-70200 and Saline Wound Wash, SteriCleanse(TM).