Ltbio Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 2
What Ltbio Co., Ltd. makes
Ltbio Co., Ltd. manufactures the OLIZ LTB-1000A, a medical device designed for [specific application not detailed in data]. This product falls under a specialized category of diagnostic or therapeutic tools, though its exact function is not specified in the provided information.
The OLIZ LTB-1000A is classified as a Class II device under regulatory frameworks and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
- Registry: GUDID
Oliz Ltb-1000A Ref K221189
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 695148479
Frequently asked questions
How many devices does Ltbio Co., Ltd. have in the registry?
The registry currently lists 2 devices for Ltbio Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ltbio Co., Ltd.'s devices?
Among its 2 most recently registered devices, Ltbio 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 Ltbio Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ltbio Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ltbio Co., Ltd. in the registry?
The most recently registered devices listed for Ltbio Co., Ltd. include OLIZ LTB-1000A.