Derma-Lock Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Derma-Lock Medical Corp. makes
Derma-Lock Medical Corp. manufactures wound closure devices, including the EPI-LOCK™ PRIMADERM, a system designed for securing dressings and protecting wounds. These products are intended for use in medical settings to maintain wound integrity and reduce infection risk.
The company’s portfolio is regulated under FDA Class I devices, with products authorised via the 510(k) pathway. Devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Multiple Ref K831204
Regimes: 510(k) Registry: 510(k)Epi-Lock T.M. Primaderm Ref K874291
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Derma-Lock Medical Corp. have in the registry?
The registry currently lists 2 devices for Derma-Lock Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Derma-Lock Medical Corp.'s devices?
Among its 2 most recently registered devices, Derma-Lock Medical Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Derma-Lock Medical Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Derma-Lock Medical Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Derma-Lock Medical Corp. in the registry?
The most recently registered devices listed for Derma-Lock Medical Corp. include MULTIPLE and EPI-LOCK T.M. PRIMADERM.