Closure Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 5
What Closure Medical Corp. makes
Closure Medical Corp. makes skin closure systems, liquid adhesives, and topical adhesives for wound care and oral relief, including the Prineo Skin Closure System, Octyldent (2-octyl cyanoacrylate), Liquidderm Liquid Adhesive Bandage, Soothe-N-Seal Canker Sore Relief, and Dermabond Topical Skin Adhesive.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) and PMA registries. The company is based in the United States.
Catalogue
Prineo Skin Closure System Ref DEN090005
Regimes: De Novo Registry: De NovoOctyldent (2-Octyl Cyanoacrylate), 02A01 Ref K980159
Regimes: 510(k) Registry: 510(k)Liquiderm Liquid Adhesive Bandage Ref K002338
Regimes: 510(k) Registry: 510(k)Soothe-N-Seal Canker Sore Relief Ref K991923
Regimes: 510(k) Registry: 510(k)Dermabond Topical Skin Adhesive Ref P960052
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Closure Medical Corp. have in the registry?
The registry currently lists 5 devices for Closure Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Closure Medical Corp.'s devices?
Among its 5 most recently registered devices, Closure Medical Corp. has devices listed in FDA 510(k) (4 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Closure Medical Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Closure Medical Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Closure Medical Corp. in the registry?
The most recently registered devices listed for Closure Medical Corp. include PRINEO SKIN CLOSURE SYSTEM, OCTYLDENT (2-OCTYL CYANOACRYLATE), 02A01, LIQUIDERM LIQUID ADHESIVE BANDAGE and SOOTHE-N-SEAL CANKER SORE RELIEF.