Sancella, Inc.
CanadaFDA applicant, unverified
- Devices
- 5
What Sancella, Inc. makes
Sancella, Inc. manufactures MEDI GUARD disposable medical barrier products including underpads, pillowcases, drapes, sheets/underlays, and dental bibs.
The company's products are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Sancella, Inc. is based in the US.
Catalogue
Medi Guard Underpad Ref K911952
Regimes: 510(k) Registry: 510(k)Medi Guard Pillowcase Ref K911948
Regimes: 510(k) Registry: 510(k)Medi Guard Drapes Ref K911950
Regimes: 510(k) Registry: 510(k)Medi Guard Sheets/Underlays Ref K911953
Regimes: 510(k) Registry: 510(k)Medi Guard Dental Bib Ref K911944
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sancella, Inc. have in the registry?
The registry currently lists 5 devices for Sancella, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sancella, Inc.'s devices?
Among its 5 most recently registered devices, Sancella, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Sancella, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Sancella, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sancella, Inc. in the registry?
The most recently registered devices listed for Sancella, Inc. include MEDI GUARD UNDERPAD, MEDI GUARD PILLOWCASE, MEDI GUARD DRAPES and MEDI GUARD SHEETS/UNDERLAYS.