FDA applicant

Triton Technology, Inc.

Salem, OH4 decisions1988–19930 recalls

FDA records 4 decisions for Triton Technology, Inc. (Salem, OH) from 1988 to 1993: 4 510(k) clearances. Most are in product codes FCK (Instrument, Biopsy, Suction) and BYZ (Trap, Sterile Specimen). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided Triton Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Triton Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Triton Technology, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Triton”

FDA records each applicant name separately; these may or may not be the same firm.

Triton Biosciences, Inc. 1 Triton Medical, LLC 1

Triton Technology, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Triton”