Lorvic Corp.
United StatesFDA applicant, unverified
- Devices
- 6
What Lorvic Corp. makes
Lorvic Corp. manufactures single-use medical devices including an impulse heat sealer for wound care, disposable compressed fibre wafers for absorption, UV germicidal units for sterilisation, saliva ejectors for oral procedures, and fluoride gel trays for dental applications. Their portfolio also covers protective shields for clinical use.
The company’s devices are regulated under FDA’s 510(k) pathway, with products classified as Class I and Class II. They are listed in the FDA’s 510(k) database and operate from the United States.
Catalogue
Impulse Heat Sealer Ref K760121
Regimes: 510(k) Registry: 510(k)Disp. Absorbent Compressed Fibre Wafer Ref K770063
Regimes: 510(k) Registry: 510(k)Shield Ref K780263
Regimes: 510(k) Registry: 510(k)Fluoride Gel Disposable Tray Ref K770064
Regimes: 510(k) Registry: 510(k)U. V. Germicidal Unit Ref K871615
Regimes: 510(k) Registry: 510(k)Saliva Ejector Ref K760620
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lorvic Corp. have in the registry?
The registry currently lists 6 devices for Lorvic Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lorvic Corp.'s devices?
Among its 6 most recently registered devices, Lorvic Corp. has devices listed in FDA 510(k) (6 devices).
What risk classes do Lorvic Corp.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Lorvic Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lorvic Corp. in the registry?
The most recently registered devices listed for Lorvic Corp. include IMPULSE HEAT SEALER, DISP. ABSORBENT COMPRESSED FIBRE WAFER, SHIELD and FLUORIDE GEL DISPOSABLE TRAY.