Sasmar, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Sasmar, Inc. makes
Sasmar, Inc. manufactures intrauterine devices (IUDs), including the CONCEIVE PLUS and the SASMAR ORIGINAL and SASMAR CLASSIC models. These devices are designed for long-term contraception and are inserted into the uterus to prevent pregnancy.
The company’s portfolio is regulated under FDA Class II devices, with product authorisation supported by 510(k) clearances. These devices are listed in the FDA’s 510(k) registry. Sasmar, Inc. is based in the United States.
Catalogue
Conceive Plus Ref K131355
Regimes: 510(k) Registry: 510(k)Sasmar Original, Sasmar Classic Ref K131084
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sasmar, Inc. have in the registry?
The registry currently lists 2 devices for Sasmar, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sasmar, Inc.'s devices?
Among its 2 most recently registered devices, Sasmar, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Sasmar, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sasmar, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sasmar, Inc. in the registry?
The most recently registered devices listed for Sasmar, Inc. include CONCEIVE PLUS and SASMAR ORIGINAL, SASMAR CLASSIC.