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Data / Medical devices / United States / Tri-Tech Forensics, Inc.

Tri-Tech Forensics, Inc.: FDA-registered device maker in Leland, NC, United States, 5 510(k) clearances

Tri-Tech Forensics, Inc. is registered with the FDA (registration 1036781) in Leland, NC, United States. It lists 19 device types. The FDA files 5 510(k) clearances under its listings, the newest dated June 16, 1997. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1036781
FEI number
1000111918
Address
3811 International Blvd NE Suite 100, Leland, NC, United States, 28451
Owner or operator
Tri-Tech Forensics, Inc. (10028837)
Roles
Manufacturer, Repackager or relabeler, Specification developer
First device listed
March 11, 2009
Registered through
2026
Brand names listed
ALERRT Victim & Responder Kit, Active Shooter Event Casualty Response Kit, Advanced Foot Care Module, Advanced Medications Module, Advanced Wound Treatment Module, BioHoop, Bleeding Control Kit, Bleeding Control Kit (Public Access) and more

Devices it lists

DeviceProduct codeClassRoleSource
Bandage, ElasticFQM1Manufacturer, Specification developeraccessdata.fda.gov
Basin, EmesisFNY1Manufactureraccessdata.fda.gov
Burn Kit Without DrugOJJ1Repackager or relabeleraccessdata.fda.gov
Container, Liquid Medication, GraduatedKYW1Specification developeraccessdata.fda.gov
Container, Specimen, SterileFMH1Repackager or relabeleraccessdata.fda.gov
First Aid Kit With DrugLRRNRepackager or relabeleraccessdata.fda.gov
First Aid Kit Without DrugOHO1Repackager or relabeleraccessdata.fda.gov
Kit, Screening, UrineJXA1Manufactureraccessdata.fda.gov
Laceration TrayPKD1Repackager or relabeleraccessdata.fda.gov
Laryngoscope, RigidCCW1Specification developeraccessdata.fda.gov
Needle, Aspiration And Injection, DisposableGAA1Repackager or relabeleraccessdata.fda.gov
Oxygen Administration KitOGL2Repackager or relabeleraccessdata.fda.gov
Splint, Extremity, Non-Inflatable, External, Non-SterileNOC1Manufacturer, Specification developeraccessdata.fda.gov
Splint, TractionHSP1Manufacturer, Specification developeraccessdata.fda.gov
Stretcher, Hand-CarriedFPP1Manufacturer, Specification developeraccessdata.fda.gov
Tourniquet KitOJS1Repackager or relabeleraccessdata.fda.gov
Tourniquet, NonpneumaticGAX1Manufacturer, Specification developeraccessdata.fda.gov
Tray, Blood CollectionGJE2Manufactureraccessdata.fda.gov
Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA2Manufacturer, Specification developeraccessdata.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 16, 1997K971111TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPERJKASubstantially EquivalentTri-Tech, Inc.accessdata.fda.gov
June 20, 1995K952246TRI-TECHIN. CUSTOM BLOOD AND/OR URINE TRANSPORT KITJXASubstantially EquivalentTri-Tech, Inc.accessdata.fda.gov
February 17, 1994K922343TRI-TECH INC. CUSTOM SEXUAL ASSAULT KITJKAUnknownTri-Tech, Inc.accessdata.fda.gov
August 27, 1993K922342TRI-TECH INC. CUSTOM BLOOD ALCOHOLJKAUnknownTri-Tech, Inc.accessdata.fda.gov
September 17, 1990K900983TRI-TECH URINE SPECIMEN KITFMHSubstantially EquivalentTri-Tech, Inc.accessdata.fda.gov

Compare with other makers

Updated June 16, 1997. 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.