INTEX TECHNOLOGIES, LLC

FDA Device Registration & Listing · Hudsonville, MI, US · Registration 3009700023

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
3009700023
FEI Number
3009700023
Entity Name
INTEX TECHNOLOGIES, LLC
City/State/Country
Hudsonville, MI, US
Establishment Address
3133 Highland Blvd., Hudsonville, MI 49426, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Intex Technologies, LLC (Owner Number: 10088531)
Owner / Operator Contact Address
3133 Highland Blvd., Hudsonville, MI 49426, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ELEVATE Patient Positions

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMP Protector, Skin Pressure General Hospital Class 1 880.6450 2023-08-24

Official Correspondent

Steve Colvin

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Intex Technologies, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3004632523 Eduard Gerlach Gmbh Luebbecke North Rhine-Westphalia, DE
3038624835 DONGGUAN HEECOOL TECHNOLOGY CO., LTD. Dongguan Guangdong, CN
3010364377 Flexor SA Barbera del Valles Barcelona, ES
3016232365 SHENZHEN FOAMTECH CO., LTD Shenzhen Guangdong, CN
2184046 OSBORN MEDICAL CORPORATION CENTENNIAL, CO, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009700023. Last updated year: 2026. Please use registration number 3009700023 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.