# Praxis Powder Technology, Inc. (contract manufacturer, Queensbury, NY): 5 new FDA device listings, incl. cerclage, fixation

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Praxis Powder Technology, Inc. |
| Owner / operator | Praxis Technology |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Queensbury, NY, US |
| New listings | 5 |
| Devices | Cerclage, Fixation; Washer, Bolt Nut; Fastener, Fixation, Nondegradable, Soft Tissue; Subcutaneous Implanted Apheresis Port |
| Product codes | JDQ, HTN, MBI, PTD |
| Device classes | Class II |
| Medical specialties | Orthopedic, General Hospital |
| First new listing | 2026-06-09 |
| Latest new listing | 2026-06-09 |
| FDA registration number | 3007304202 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.