Sunbio, Inc.
South KoreaFDA applicant, unverified FDA
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
MucoPEG Ref K190144
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 689393098
FDA establishments
- Sunbio, Inc. Incheon-si · KR FEI 3013534361
Frequently asked questions
How many devices does Sunbio, Inc. have in the registry?
The registry currently lists 2 devices for Sunbio, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sunbio, Inc.'s devices?
Among its 2 most recently registered devices, Sunbio, Inc. 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 are the newest devices from Sunbio, Inc. in the registry?
The most recently registered devices listed for Sunbio, Inc. include MucoPEG™ SBMD-MU-001 and MucoPEG.
Which FDA establishments are linked to Sunbio, Inc.?
1 FDA establishment is linked to Sunbio, Inc. in the registry; they are listed on the company page.