Oneday Biotech Co., Ltd.
South KoreaFDA applicant, unverified FDA FEI 3017548645
- Devices
- 75
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Oneday Biotech Co., Ltd. makes
Oneday Biotech Co., Ltd. manufactures dental implant components, including the Oneday Implant Abutment and the Oneday Mini Implant System, designed for use in oral and maxillofacial procedures.
These devices are classified as Class II under regulatory frameworks, with submissions recorded in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Search and filter all 75 devicesShowing 1-50 of 75
Company details
- FDA FEI number
- 3017548645
- DUNS number
- 694607898
- Address
- 135 C SEONGSEODONGRO DALSEOGU, DAEGU
Frequently asked questions
How many devices does Oneday Biotech Co., Ltd. have in the registry?
The registry currently lists 75 devices for Oneday Biotech Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oneday Biotech Co., Ltd.'s devices?
Among its 50 most recently registered devices, Oneday Biotech Co., Ltd. has devices listed in FDA GUDID (50 devices).
What risk classes do Oneday Biotech Co., Ltd.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Oneday Biotech Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oneday Biotech Co., Ltd. in the registry?
The most recently registered devices listed for Oneday Biotech Co., Ltd. include I Do S3813C, I Do S3815C, I Do S4015C and I Do S4508C.