This page includes the latest FDA filings for Diamond Tool Manufacturing. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3003048504 |
| FEI Number | 3003048504 |
| Name | DIAMOND TOOL MANUFACTURING |
| Owner & Operator | Diamond Tool Manufacturing |
| Contact Address | 14540 Jib Plymouth MI 48170 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 14540 Jib St Plymouth, MI 48170 US |
| Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
|---|---|---|
DIAMOND TOOL MANUFACTURING | Surgical Bur | 2016-02-16 |