PRAXIS POWDER TECHNOLOGY, INC.

FDA Device Registration & Listing · Queensbury, NY, US · Registration 3007304202

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3007304202
FEI Number
3007304202
Entity Name
PRAXIS POWDER TECHNOLOGY, INC.
City/State/Country
Queensbury, NY, US
Establishment Address
604 Queensbury Ave, Queensbury, NY 12804, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Praxis Technology (Owner Number: 10053738)
Owner / Operator Contact Address
604 Queensbury Avenue, Queensbury, NY 12804, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Locking Button

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HTN Washer, Bolt Nut Orthopedic Class 2 888.3030 2017-01-06
JDQ Cerclage, Fixation Orthopedic Class 2 888.3010 2026-06-09
MBI Fastener, Fixation, Nondegradable, Soft Tissue Orthopedic Class 2 888.3040 2022-03-11
MBI Fastener, Fixation, Nondegradable, Soft Tissue Orthopedic Class 2 888.3040 2026-06-09
PTD Subcutaneous Implanted Apheresis Port General Hospital Class 2 880.5965 2026-06-09
HTN Washer, Bolt Nut Orthopedic Class 2 888.3030 2026-06-09

Official Correspondent

Jobe Piemme

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Praxis Technology
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K874919 Orthomet, Inc. ORTHOMET WIRE FOR SUTURE, CERCLAGE 1988-01-07
K193295 Parcus Medical, LLC Parcus Knotless PEEK and PEEK CF Push-In Suture Anchor 2020-01-23
K193606 Conmed Corporation Y-Knot OneStep Anchor 2020-01-22
K984200 R. Thomas Grotz, M.D., Inc. STABILIZER SOFT TISSUE ANCHOR, 5 AND 8MM; ANCHOR INSERTER, 5 AND 8MM; STABILIZER DRILL, 5 AND 8MM, NONSTERILE; STABILIZE 1999-01-21
K171060 Riverpoint Medical OrthoButton AL 2017-06-02

Similar Registrations

Registration Number Establishment Name Location
3007923096 Changzhou Biomet Medical Devices Co., Ltd. Changzhou City Jiangsu, CN
3009417901 SYNTHES GMBH Zuchwil Solothurn, CH
3006783837 STRUCTURE MEDICAL, LLC. Naples, FL, US
3003604053 SMITH & NEPHEW INC. ANDOVER, MA, US
3008870565 Implant Logistics / AMS Micromedical Sparta, WI, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007304202. Last updated year: 2026. Please use registration number 3007304202 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.