Medin Corp.
United StatesFDA applicant, unverified
- Devices
- 5
What Medin Corp. makes
Medin Corp. manufactures self-retraction systems for surgical procedures, including rectal and general abdominal applications. Their products include the HARGIS Rectal Self Retraction System, Cradling System, and variants of the HARGIS Self-Retraction System, designed to assist in tissue management during surgery.
These devices are classified under FDA categories Class I and Class II, with regulatory clearance obtained through the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Sterilization Container Ref K833343
Regimes: 510(k) Registry: 510(k)Hargis Rectal Self Retration System Ref K921019
Regimes: 510(k) Registry: 510(k)Cradling System Ref K761032
Regimes: 510(k) Registry: 510(k)Hargis Self Retraction System Ref K921020
Regimes: 510(k) Registry: 510(k)Hargis SR2 Self-Retraction System Ref K921017
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medin Corp. have in the registry?
The registry currently lists 5 devices for Medin Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medin Corp.'s devices?
Among its 5 most recently registered devices, Medin Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Medin Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Medin Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medin Corp. in the registry?
The most recently registered devices listed for Medin Corp. include STERILIZATION CONTAINER, HARGIS RECTAL SELF RETRATION SYSTEM, CRADLING SYSTEM and HARGIS SELF RETRACTION SYSTEM.