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
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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 16, 1997 | K971111 | TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPER | JKA | Substantially Equivalent | Tri-Tech, Inc. | accessdata.fda.gov |
| June 20, 1995 | K952246 | TRI-TECHIN. CUSTOM BLOOD AND/OR URINE TRANSPORT KIT | JXA | Substantially Equivalent | Tri-Tech, Inc. | accessdata.fda.gov |
| February 17, 1994 | K922343 | TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT | JKA | Unknown | Tri-Tech, Inc. | accessdata.fda.gov |
| August 27, 1993 | K922342 | TRI-TECH INC. CUSTOM BLOOD ALCOHOL | JKA | Unknown | Tri-Tech, Inc. | accessdata.fda.gov |
| September 17, 1990 | K900983 | TRI-TECH URINE SPECIMEN KIT | FMH | Substantially Equivalent | Tri-Tech, Inc. | accessdata.fda.gov |
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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.