FDA applicant

Capintec Instruments, Inc.

Pittsburgh, PA7 decisions1991–19940 recalls

FDA records 7 decisions for Capintec Instruments, Inc. (Pittsburgh, PA) from 1991 to 1994: 7 510(k) clearances. Most are in product codes KPT (Calibrator, Dose, Radionuclide) and IZD (Probe, Uptake, Nuclear). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Capintec Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Capintec Instruments, 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 “Capintec”

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

Capintec, Inc. 14

Capintec Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Capintec”