Scandinavian Formulas, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3003547663
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Scandinavian Formulas, Inc. makes
Scandinavian Formulas, Inc. manufactures SLIVASURE, a Class I medical device designed for oral use, intended to support digestive health through probiotic formulations.
The company’s portfolio is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Slivasure Ref K051409
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3003547663
- Address
- 140 E Church St, SELLERSVILLE, PA, 18960
Frequently asked questions
How many devices does SCANDINAVIAN FORMULAS, INC. have in the registry?
The registry currently lists 1 device for SCANDINAVIAN FORMULAS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SCANDINAVIAN FORMULAS, INC.'s devices?
Among its 1 most recently registered device, SCANDINAVIAN FORMULAS, INC. has devices listed in FDA 510(k) (1 device).
What risk classes do SCANDINAVIAN FORMULAS, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for SCANDINAVIAN FORMULAS, INC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from SCANDINAVIAN FORMULAS, INC. in the registry?
The most recently registered devices listed for SCANDINAVIAN FORMULAS, INC. include SLIVASURE.