Regency Biotech
Country not established
- Devices
- 1
What Regency Biotech makes
Regency Biotech manufactures fetal bovine serum equivalents (FBS, EQ), which are used as culture media supplements in cell and tissue culture applications, supporting cell growth and maintenance in laboratory settings.
The company’s portfolio is classified under FDA’s Class I medical devices and is listed via the 510(k) pathway. The products are regulated under U.S. jurisdiction.
Catalogue
Fbs, Eq., Or Fetal Bovine Serum Equivalent Ref K884031
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Regency Biotech have in the registry?
The registry currently lists 1 device for Regency Biotech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Regency Biotech's devices?
Among its 1 most recently registered device, Regency Biotech has devices listed in FDA 510(k) (1 device).
What risk classes do Regency Biotech's devices fall under?
Among its 1 most recently registered device, the classes recorded for Regency Biotech's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Regency Biotech in the registry?
The most recently registered devices listed for Regency Biotech include FBS, EQ., OR FETAL BOVINE SERUM EQUIVALENT.