510(k) Report

FDA applicant

Healthteam

S. Plainfield, NJ8 decisions1985–19890 recalls

FDA records 8 decisions for Healthteam (S. Plainfield, NJ) from 1985 to 1989: 8 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and ILY (Lamp, Infrared, Therapeutic Heating). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Healthteam since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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