This page includes the latest FDA filings for Cre Med. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3010057648 |
| FEI Number | 3010057648 |
| Name | CRE-MED |
| Owner & Operator | CRE-MED |
| Contact Address | 4101 Masthead St. NE Albuquerque NM 87109 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 4101 Masthead St NE Albuquerque, NM 87109 US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
CRE-MED | Kinesio Tex Gold FP Wave | 2012-12-21 |
| Import ID | Shipment | Cargo Description | Quantity |
|---|---|---|---|
| 2020092548895 | Nagoya Ko ,Japan -> Los Angeles, California | KINESIO SCISSORS HS CODE 8213 00 | 20 CTN |