This page includes the latest FDA filings for Praxis Powder Technology Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3007304202 |
| FEI Number | 3007304202 |
| Name | PRAXIS POWDER TECHNOLOGY, INC. |
| Owner & Operator | Praxis Powder Technology, Inc. |
| Contact Address | 604 Queensbury Avenue Queensbury NY 12804 US |
| Official Correspondent |
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| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 604 Queensbury Ave Queensbury, NY 12804 US |
| Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
|---|---|---|
PRAXIS POWDER TECHNOLOGY, INC. | Arthrex | 2019-11-15 |
PRAXIS POWDER TECHNOLOGY, INC. | Arthrex | 2019-11-15 |
PRAXIS POWDER TECHNOLOGY, INC. | Arthrex | 2019-11-15 |
| NCAGE Code | 79PK3 | PRAXIS POWDER TECHNOLOGY INC. |
| CAGE Code | 79PK3 | PRAXIS POWDER TECHNOLOGY INC. |
| S.A.M. Registration | 79PK3 [190586672] | PRAXIS POWDER TECHNOLOGY INC. |