Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005346101

FEI Number

3005346101

Entity Name

TECHTRADE LLC

City/State/Country

Orlando, FL, US

Establishment Address

6900 Tavistock Lakes Blvd., Ste 400, Orlando, FL 32827, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

TECHTRADE LLC (Owner Number: 10029022)

Owner / Operator Contact Address

6900 Tavistock Lakes Blvd., Suite 400, Orlando, FL 32827, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K042145

PMA Number

N/A

All Registered Proprietary Names

Ready-Heat Blankets Ready-Heat Blankets Ready-Heat Blankets

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IMD	Pack, Hot Or Cold, Disposable	Physical Medicine	Class 1	890.5710	2017-03-17
KME	Bedding, Disposable, Medical	General Hospital	Class 1	880.6060	2017-03-17
IMD	Pack, Hot Or Cold, Disposable	Physical Medicine	Class 1	890.5710	2009-03-30
KME	Bedding, Disposable, Medical	General Hospital	Class 1	880.6060	2009-03-30

Official Correspondent

Erin Bart

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TECHTRADE LLC

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

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005346101. Last updated year: 2026. Please use registration number 3005346101 when referencing this establishment in official correspondence.