FDA applicant

Current Technologies, Inc.

Mchenry, IL3 decisions1980–19830 recalls

FDA records 3 decisions for Current Technologies, Inc. (Mchenry, IL) from 1980 to 1983: 3 510(k) clearances. Most are in product codes JKA (Tubes, Vials, Systems, Serum Separators, Blood…) and FMP (Protector, Skin Pressure). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Current Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Current Technologies, 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 “Current”

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

Current Health, Ltd. 5

Current Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Current”