Kedumin Kits, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Kedumin Kits, Ltd. makes
Kedumin Kits, Ltd. manufactures sterile circumcision kits designed for medical use, including the SAFEBRIS STERILE CIRCUMCISION KIT.
The company’s products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA registry. The manufacturer is based in the United States.
Catalogue
Safebris Sterile Circumcision Kit Ref K902119
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kedumin Kits, Ltd. have in the registry?
The registry currently lists 1 device for Kedumin Kits, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kedumin Kits, Ltd.'s devices?
Among its 1 most recently registered device, Kedumin Kits, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Kedumin Kits, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kedumin Kits, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kedumin Kits, Ltd. in the registry?
The most recently registered devices listed for Kedumin Kits, Ltd. include SAFEBRIS STERILE CIRCUMCISION KIT.