This page includes the latest FDA filings for K D F Inc Pro Cision Machining Manufacturing. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3009829577 |
| FEI Number | 3009829577 |
| Name | K.D.F. INC. DBA: PRO-CISION MACHINING MANUFACTURING |
| Owner & Operator | K.D.F. Inc. DBA: Pro-cision Machining Manufacturing |
| Contact Address | 15875 Concord Circle Morgan Hill CA 95037 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 15875 Concord Cir Morgan Hill, CA 95037 US |
| Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
|---|---|---|
K.D.F. INC. DBA: PRO-CISION MACHINING MANUFACTURING | Universal ACL Instrumentation | 2012-10-09 |