Sixarp LLC, Praxis

FDA Device Registration & Listing · Grand Rapids, MI, US · Registration 1000115322

Public Record Device Listing Expiry Year: 2026 AvaSpecs displays structured public-record fields for easier browsing and citation.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1000115322
FEI Number
1000115322
Entity Name
Sixarp LLC, Praxis
City/State/Country
Grand Rapids, MI, US
Establishment Address
7650 Caterpillar Ct SW Ste D, Grand Rapids, MI 49548, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Sixarp LLC, Praxis (Owner Number: 10031872)
Owner / Operator Contact Address
7650 Caterpillar Dr, Suite D, Grand Rapids, MI 49548, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NAB Gauze / Sponge,Nonresorbable For External Use General, Plastic Surgery Class 1 878.4014 2015-10-28

Official Correspondent

John Lowry

US Agent Details

No US Agent registered (Local establishment).

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000115322. Last updated year: 2026. Please use registration number 1000115322 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.
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