TECHNICAL PRODUCTS, INC.

FDA Device Registration & Listing · Buford, GA, US · Registration 1061771

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
1061771
FEI Number
1000511237
Entity Name
TECHNICAL PRODUCTS, INC.
City/State/Country
Buford, GA, US
Establishment Address
5089 Bristol Industrial Way, Suite A, Buford, GA 30518, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
TECHNICAL PRODUCTS, INC. (Owner Number: 9021587)
Owner / Operator Contact Address
5089 Bristol Industrial Way, Suite A, Buford, GA 30518, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K973166
PMA Number
N/A

All Registered Proprietary Names

Sil-Tec Thick Sheets Silicone Pennrose Drain EZ-T T-TUBES SIL-TEC OVAL SHAPES JP & Blake Drains Tracheal Cannula/EZ Sil-tec Tubing Sil-Tec Malecot Catheter SIL-TEC ROD

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MIB Elastomer, Silicone Block Ear, Nose, Throat Class 2 874.3620 2007-11-05
GCD Connector, Catheter General, Plastic Surgery Class 1 878.4200 2008-11-13
BTR Tube, Tracheal (W/Wo Connector) Anesthesiology Class 2 868.5730 2006-03-02
HXA Prosthesis, Tendon, Passive Orthopedic Class 2 888.3025 2006-03-02
GBP Catheter, Multiple Lumen General, Plastic Surgery Class 1 878.4200 2008-11-13
LRC Instrument, Ent Manual Surgical Ear, Nose, Throat Class 1 874.4420 2007-11-05
MIB Elastomer, Silicone Block Ear, Nose, Throat Class 2 874.3620 2007-10-16
FEW Catheter, Malecot Gastroenterology, Urology Class 2 876.5090 2007-11-05
MIB Elastomer, Silicone Block Ear, Nose, Throat Class 2 874.3620 2006-03-02

Official Correspondent

Marguerite Thompson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TECHNICAL PRODUCTS, INC.
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
K233341 Covidien, LLC Shiley™ Oral/Nasal Endotracheal Tube Intermediate Cuff, Non-DEHP (87430, 87435, 87440, 87445, 87450, 87455, 87460, 87465, 87470, 87475, 87480, 87485, 87490, 87495, 87410) 2024-05-20
K243785 Covidien, LLC Shiley™ Oral/Nasal Tracheal Tube with TaperGuard™ Cuff Reinforced, Murphy Eye Shiley™ Tracheal Tube TaperGuard™ Cuff Reinforced with Stylet Shiley™ Lo-Contour Oral/Nasal Tracheal Tube Cuffed Reinforced Shiley™ Lo-Contour Oral/Nasal Tracheal Tube Cuffed Reinforced, Murphy Eye Shiley™ Oral/Nasal Tracheal Tube Cuffless Reinforced 2025-09-25
K243477 Askorn Medical Universal Tendon Spacer 2025-01-10
K143738 Intuit Medical Products, LLC DSS Sinusplasty Balloon Catheter 2015-08-27

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1061771. Last updated year: 2026. Please use registration number 1061771 when referencing this establishment in official correspondence.
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