Skingrab Co., Ltd.
South KoreaFDA applicant, unverified FDA
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
Catalogue
- Registry: GUDID
Finiff System Ref K242688
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Skingrab GEUMCHEON-GU Seoul · KR FEI 3041276883
Frequently asked questions
How many devices does Skingrab Co., Ltd. have in the registry?
The registry currently lists 2 devices for Skingrab Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Skingrab Co., Ltd.'s devices?
Among its 2 most recently registered devices, Skingrab Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Skingrab Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Skingrab Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Skingrab Co., Ltd. in the registry?
The most recently registered devices listed for Skingrab Co., Ltd. include FINIFF SYSTEM.
Which FDA establishments are linked to Skingrab Co., Ltd.?
1 FDA establishment is linked to Skingrab Co., Ltd. in the registry; they are listed on the company page.