Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1036781

FEI Number

1000111918

Entity Name

TRI-TECH FORENSICS, INC.

City/State/Country

Leland, NC, US

Establishment Address

3811 International Blvd NE, Suite 100, Leland, NC 28451, US

Establishment Type(s)

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

Owner / Operator

Tri-Tech Forensics, Inc. (Owner Number: 10028837)

Owner / Operator Contact Address

3811 International Blvd NE, Suite 100, Leland, NC 28451, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Burn Treatment Module (individual) Burn Treatment Module Trauma Cap Tri-Tech Forensics Urine Specimen Kit Tri-Fold Minor First Aid Kit Wildland Fire Personal First Aid Kit Advanced Medications Module The Nick Fixer Personal Plus" First Aid Kit Rescue Essentials Wilderness First Aid Kit Northern Tier Kit For Scout Leaders Medications Unit Dose Pack O2 Delivery Kit BioHoop Tri-Tech Forensics Custom Blood Alcohol Kit BriteView Personal Protection Module Advanced Foot Care Module Vehicle First Aid Kit Rescue Essentials First Responder Pack Blister Kit Universal First Aid Refill Kit Police Officer's Pocket Trauma Kit Hunter Safety Kit Immobilization module First Responder Kit US Customs & Border Protection First Responder Medical Bag Pandemic Protection Module Minor First Aid Kit Tactical Medic Kit Range Master Medical Kit Active Shooter Event Casualty Response Kit Concealed Carry Trauma Kit (QuikClot LE Version) Patrol Officer's Pocket Trauma Kit Bleeding Control Kit Mutual Aid Trauma Kit Motorcycle Operator Kit Responder Trauma Kit (Celox Rapid Version) Rescue Essentials Tactical Ankle Medical Kit Rescue Essentials Downed Officer Kit Tactical First Response Kit - Basic School Resource Officer Mass Casualty Kit Plain Clothes Carry Medical Kit Outdoor Range Medical Kit - Advanced Responder Trauma Kit (Combat Gauze LE Version) Tactical Development Group Training Kit School Resource Officer Pocket Trauma Kit Covert Carry Advanced Trauma Kit ALERRT Victim & Responder Kit Plain clothes Carry Medical Kit (Celox Rapid Version) Bleeding Control Kit (Public Access) Outdoor Range Medical Kit - Tactical Classroom Critical Incident Response Kit US Customs & Border Protection Individual First Aid Kit Tactical First Response Kit - Advanced Rapid Response Kit- Rescue Task Force Edition Concealed Carry Trauma Kit (Celox Rapid Version) US Customs & Border Protection Casualty Response Kit Tri-Tech Forensics Evacuated Blood Collection Tube, Gray Stopper TPAK Needle Decompression Kit Enhanced Pneumodart Needle Slishman Traction Splint (STS) STS-C Slishman Compact Traction Splint Slishman Traction Splint Gen 2 STS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OJJ	Burn Kit Without Drug	General, Plastic Surgery	Class 1	878.4022	2018-12-07
FQM	Bandage, Elastic	General Hospital	Class 1	880.5075	2023-09-05
FMH	Container, Specimen, Sterile	Pathology	Class 1	864.3250	2009-03-11
LRR	First Aid Kit With Drug	Unknown	Class N	N/A	2018-12-07
OGL	Oxygen Administration Kit	Anesthesiology	Class 2	868.5655	2018-12-07
FNY	Basin, Emesis	General Hospital	Class 1	880.6730	2024-02-21
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2009-03-11
CCW	Laryngoscope, Rigid	Anesthesiology	Class 1	868.5540	2024-02-19
OHO	First Aid Kit Without Drug	General, Plastic Surgery	Class 1	878.4014	2018-12-07
OJS	Tourniquet Kit	General, Plastic Surgery	Class 1	878.5900	2018-12-07
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2009-03-11
GAA	Needle, Aspiration And Injection, Disposable	General, Plastic Surgery	Class 1	878.4800	2025-08-15
HSP	Splint, Traction	Orthopedic	Class 1	888.5890	2018-12-07

Official Correspondent

Eric Barton

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Tri-Tech Forensics, 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
K945777	Smiths Industries Medical Systems, Inc.	PRO-VENT(TM), PULSATOR(R), AND LINE DRAW(TM) ARTERIAL BLOOD SAMPLING SYRINGES	1994-12-22
K781371	Ferris Mfg. Corp.	BONE MARROW ASPIRATION KIT	1978-09-20

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0030-2014	Perkin Elmer Health Sciences, Inc.	2	Perkin Elmer 226 Sample Collection Device, Serial numbers: 06132903 - 06198900. The PerkinElmer 226 Sample Collection Devices are intended to be used as a medium to collect and transport whole blood specimen spots to a laboratory, in newborn screening. The device includes a tear-apart form for the collection of demographic information.
Z-0144-2024	Covidien	1	Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
Z-0168-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only
Z-0169-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only
Z-0017-2023	Hobbs Medical, Inc.	1	Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1036781. Last updated year: 2026. Please use registration number 1036781 when referencing this establishment in official correspondence.