This page includes the latest FDA filings for Woojeon Co. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3010201636 | ||||||||
| FEI Number | 3010201636 | ||||||||
| Name | Peter Chung | ||||||||
| Owner & Operator | Woojeon Co. | ||||||||
| Contact Address | 2F, 3F, 85-22, Sanbon-ro, Gunpo-si KR-41 Gyeonggido 435-832 KR | ||||||||
| Official Correspondent |
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| US Agent |
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| Importing Logistics Registration |
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| Registration Status | 1 | ||||||||
| Initial Importer | N | ||||||||
| Registration Expiration | 2020-04-25 | ||||||||
| Registration Address | 300 Atwood sSt. Pittsburgh, PA 15213 US | ||||||||
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
Peter Chung [Woojeon Co.] | WOOJEON ACUPUNCTURE NEEDLE | 2012-12-19 |
WOOJEON COMPANY | WOOJEON ACUPUNCTURE NEEDLE (=SERA ACUPUNCTURE NEEDLE) | 2011-11-04 |