510(k) Report

FDA applicant

Beacon Converters, Inc.

Mchenry, IL2 decisions1981–19810 recalls

FDA records 2 decisions for Beacon Converters, Inc. (Mchenry, IL) in 1981: 2 510(k) clearances. Most are in product codes JOJ (Indicator, Physical/Chemical Sterilization…) and KCT (Sterilization Wrap Containers, Trays…). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Beacon Converters, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • JOJIndicator, Physical/Chemical Sterilization Process1decision
  • KCTSterilization Wrap Containers, Trays, Cassettes & Other Accessories1decision

What has FDA decided for it lately?

  • K811408Sterilization Indicator/Seal ProtectorBeacon Converters, Inc. · 1981
  • K810469Steriledge Self Seal PouchBeacon Converters, Inc. · 1981

All 2 as Beacon Converters, Inc. →

Other applicant names beginning “Beacon”

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

Beacon Laboratories, Inc. 18Beacon Biosignals, Inc. 4Beacon Surgical, Inc. 2Beacon Biologicals, Inc. 1Beacon Endoscopic 1