Data / Medical devices / South Korea / Dongbang Medical Co. Ltd.
Dongbang Medical Co. Ltd.: FDA-registered device maker in BORYEONG-SI Chungnam, South Korea, 2 510(k) clearances
Dongbang Medical Co. Ltd. is registered with the FDA (registration 3002497459) in BORYEONG-SI Chungnam, South Korea. It lists 5 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 20, 2007. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3002497459
- Address
- 40, 30, Saneopdanji-gil, Ungcheon-eup, BORYEONG-SI Chungnam, South Korea, 355-851
- Owner or operator
- DongBang Medical Co. Ltd. (9096684)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler
- First device listed
- July 23, 2008
- Registered through
- 2026
- Brand names listed
- Bong Rae Moxa, Charcoal Moxa Cone, DB FNS, DB FNS & Dr. Back 10 Story (FN-1) Micro Needle, DB Meditouch, DB Meditouch Needles, DBC, DBC Detox-5 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Pressure Applying | KNM | 1 | Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Needle, Acupuncture, Single Use | MQX | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Needle, Suturing, Disposable | GAB | 1 | Manufacturer | accessdata.fda.gov |
| Pack, Heat, Moist | IMA | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 20, 2007 | K070917 | FEEL-JECT INSULIN SYRINGE | FMF | Substantially Equivalent | Feel Tech | accessdata.fda.gov |
| May 4, 1999 | K990328 | DBC, DONG BANG ACUPUNCTURE NEEDLES | MQX | Substantially Equivalent | Morning Star, Dong Bang Acupuncture U.S.A., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Needle, Acupuncture, Single Use
- All makers of Needle, Suturing, Disposable
- All makers of Pack, Heat, Moist
- All makers of Syringe, Piston
- All makers of Device, Pressure Applying
Updated June 20, 2007. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.