Laivan Corp.
United StatesFDA applicant, unverified
- Devices
- 6
What Laivan Corp. makes
Laivan Corp. makes waterproof breathable covers, porous elastic covers, and surgical gowns, including products such as POLYDERM WBC (TM), POLYDERM PEC(TM), POLYDERM A+B(TM), AQUADERM, and TOTAL PROTECTIVE BREATHEABLE SURGICAL GOWNS, along with modified labeling for POLYDERM WBC(TM).
The company's devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; Laivan Corp. is based in the United States.
Catalogue
Polyderm Wbc (Tm), Waterproof Breathable Cover Ref K880206
Regimes: 510(k) Registry: 510(k)Aquaderm Ref K885205
Regimes: 510(k) Registry: 510(k)Modified Labeling For Polyderm Wbc(Tm) Ref K890940
Regimes: 510(k) Registry: 510(k)Polyderm Pec(Tm), Porous Elastic Cover Ref K880964
Regimes: 510(k) Registry: 510(k)Polyderm A+b(Tm) Ref K880153
Regimes: 510(k) Registry: 510(k)Total Protective Breatheable Surgical Gowns Ref K923815
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laivan Corp. have in the registry?
The registry currently lists 6 devices for Laivan Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laivan Corp.'s devices?
Among its 6 most recently registered devices, Laivan Corp. has devices listed in FDA 510(k) (6 devices).
What risk classes do Laivan Corp.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Laivan Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laivan Corp. in the registry?
The most recently registered devices listed for Laivan Corp. include POLYDERM WBC (TM), WATERPROOF BREATHABLE COVER, AQUADERM, MODIFIED LABELING FOR POLYDERM WBC(TM) and POLYDERM PEC(TM), POROUS ELASTIC COVER.