Hancock Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Hancock Laboratories, Inc. makes
Hancock Laboratories, Inc. manufactures surgical sutures, including Mersilene sutures, and vascular access products such as the Duran Flexible Ring and Modified Catheter Package. The company also produces obturators, including Hancock Obturators, and vascular tools like the Hancock Aortic Punch.
The portfolio includes devices classified as Class I and Class II under FDA regulations, with several products listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Duran Flexible Ring Ref K780568
Regimes: 510(k) Registry: 510(k)Modified Catheter Package Ref K800703
Regimes: 510(k) Registry: 510(k)Hancock * Obturators Ref K801885
Regimes: 510(k) Registry: 510(k)Mersilene Sutures Ref K790534
Regimes: 510(k) Registry: 510(k)Hancock Aortic Punch Ref K800122
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hancock Laboratories, Inc. have in the registry?
The registry currently lists 5 devices for Hancock Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hancock Laboratories, Inc.'s devices?
Among its 5 most recently registered devices, Hancock Laboratories, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Hancock Laboratories, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Hancock Laboratories, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hancock Laboratories, Inc. in the registry?
The most recently registered devices listed for Hancock Laboratories, Inc. include DURAN FLEXIBLE RING, MODIFIED CATHETER PACKAGE, HANCOCK * OBTURATORS and MERSILENE SUTURES.