MEDNIUM CORPORATION

FDA Device Registration & Listing · El Paso, TX, US · Registration 3013658769

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
3013658769
FEI Number
3013658769
Entity Name
MEDNIUM CORPORATION
City/State/Country
El Paso, TX, US
Establishment Address
109 E Redd Rd, El Paso, TX 79932, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Mednium Corporation (Owner Number: 10054850)
Owner / Operator Contact Address
109 Redd Rd, Unit TC356, El Paso, TX 79912, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

LiftClear WarmClear Trocar PierceClear GraspClear

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GDI Dissector, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2017-09-26
IMD Pack, Hot Or Cold, Disposable Physical Medicine Class 1 890.5710 2025-12-22
GEA Cannula, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2017-07-22
FZX Guide, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2017-08-08
HCF Instrument, Ligature Passing And Knot Tying General, Plastic Surgery Class 1 878.4800 2017-07-22

Official Correspondent

Robert Bromley

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mednium Corporation
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
K880871 John Wagner Associates, Inc. GRABBER WARM PACK/MINI MINI HEATER/FOOT HEATER 1988-05-20
K863293 Lifestream Int'L, Inc. DISPOSABLE SUCTION CANNULA NO. 902008-000 1986-09-09

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0505-2022 Philips North America Llc 1
Infa-Therm Transport Mattress, Reference Number 989805616831 1015
Z-0506-2022 Philips North America Llc 1
Infant Heel Warmers w/strap, Reference # 989805603201 1223

Similar Registrations

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3013602181 Blink Medical LTD Solihull, GB
8010159 A. SCHWEICKHARDT GMBH & CO. KG Seitingen-Oberflacht Baden-Wurttemberg, DE
1045379 STEPHENS INSTRUMENTS, INC LEXINGTON, KY, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013658769. Last updated year: 2026. Please use registration number 3013658769 when referencing this establishment in official correspondence.
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