Skip to the page

Data / Medical devices / United States / Technical Products, Inc.

Technical Products, Inc.: FDA-registered device maker in Buford, GA, United States, 7 510(k) clearances

Technical Products, Inc. is registered with the FDA (registration 1061771) in Buford, GA, United States. It lists 10 device types. The FDA files 7 510(k) clearances under its listings, the newest dated June 4, 2002. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
1061771
FEI number
1000511237
Address
5089 Bristol Industrial Way, Suite A, Buford, GA, United States, 30518
Owner or operator
TECHNICAL PRODUCTS, INC. (9021587)
Roles
Manufacturer, Repackager or relabeler
First device listed
March 2, 2006
Registered through
2026
Brand names listed
EZ-T T-TUBES, JP & Blake Drains, SIL-TEC OVAL SHAPES, SIL-TEC ROD, Sil-Tec Incision Drains, Sil-Tec Malecot Catheter, Sil-Tec Sheeting, Sil-Tec Thick Sheets and more

Devices it lists

DeviceProduct codeClassRoleSource
Apparatus, Suction, Single Patient Use, Portable, NonpoweredGCY1Repackager or relabeleraccessdata.fda.gov
Catheter, IrrigationGBX1Repackager or relabeleraccessdata.fda.gov
Catheter, MalecotFEW2Repackager or relabeleraccessdata.fda.gov
Catheter, Multiple LumenGBP1Repackager or relabeleraccessdata.fda.gov
Connector, CatheterGCD1Repackager or relabeleraccessdata.fda.gov
Elastomer, Silicone BlockMIB2Manufacturer, Repackager or relabeleraccessdata.fda.gov
Instrument, Ent Manual SurgicalLRC1Manufactureraccessdata.fda.gov
Mesh, Surgical, PolymericFTL2Manufacturer, Repackager or relabeleraccessdata.fda.gov
Prosthesis, Tendon, PassiveHXA2Repackager or relabeleraccessdata.fda.gov
Tube, Tracheal (W/Wo Connector)BTR2Repackager or relabeleraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
June 4, 2002K013321SILICONE TRACHEAL T-TUBESBTRSubstantially EquivalentTechnical Products, Inc.accessdata.fda.gov
December 5, 1997K973385OVAL SHAPESHXASubstantially EquivalentTechnical Products, Inc.accessdata.fda.gov
November 21, 1997K973166DOW CORNING SILASTIC ELASTOMER Q7-4750MIBSubstantially EquivalentTechnical Products, Inc.accessdata.fda.gov
July 1, 1997K971472SIL-TEC NONREINFORCED SHEETING, REINFORCED SHEETING, RADIOPAQUE SHEETING, REINFORCED RADIOPAQUE SHEETING, EXTRA FIRM GRAFTLSubstantially EquivalentTechnical Products, Inc.accessdata.fda.gov
May 22, 1997K971613SIL-TEC SMALL/LARGE BORE TUBING/SIL-TEC HIGH DUROMETER TUBING/SIL-TEC RADIOPAQUE TUBINGMIBSubstantially EquivalentTechnical Products, Inc.accessdata.fda.gov
May 22, 1996K961081SPIRIT RIDGE SILICONE CARVING BLOCKMIBSubstantially EquivalentRand Scientific Corp.accessdata.fda.gov
November 6, 1995K954116SILICONE MALECOT CATHETER WITH PEZZER/MUSHROOM TIPFEWSubstantially EquivalentTechnical Products, Inc.accessdata.fda.gov

Compare with other makers

Updated June 4, 2002. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.