Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3038252369

FEI Number

3038252369

Entity Name

TRINETICS GROUP

City/State/Country

Melbourne, FL, US

Establishment Address

3153 Skyway Cir, Melbourne, FL 32934, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Trinetics Group (Owner Number: 10093357)

Owner / Operator Contact Address

3153 Skyway Circle, Melbourne, FL 32934, US

Initial Importer Flag

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
MDM	Instrument, Manual, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2025-05-05

Official Correspondent

Eric Stern

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Trinetics Group

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 3038252369. Last updated year: 2026. Please use registration number 3038252369 when referencing this establishment in official correspondence.