Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3039405687

FEI Number

3039405687

Entity Name

TRINYTYEC

City/State/Country

Valaurie Drome, FR

Establishment Address

1 rue Pierre et Marie Curie, Valaurie Drome 26230, FR

Establishment Type(s)

Remanufacture Medical Device,Repack or Relabel Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

TRINYTYEC (Owner Number: 10093678)

Owner / Operator Contact Address

1 rue Pierre et Marie Curie, Valaurie, FR-26 26230, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DEVICE, PROSTHESIS ALIGNMENT

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IQO	Device, Prosthesis Alignment	Physical Medicine	Class 1	890.3025	2025-06-20

Official Correspondent

Stephane Paillet

US Agent Details

Glenn Choi Email: gchoi2001@yahoo.com Phone: (714) 5240663

Related Public Records

Same Entity

TRINYTYEC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3039405687. Last updated year: 2026. Please use registration number 3039405687 when referencing this establishment in official correspondence.