510(k) Report

FDA applicant

Inter Continental Health Care

Boston, MA2 decisions1989–19890 recalls

FDA records 2 decisions for Inter Continental Health Care (Boston, MA) in 1989: 2 510(k) clearances. All are in product code LYY (Latex Patient Examination Glove). 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 Inter Continental Health Care’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inter Continental Health Care since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Inter Continental Health Care 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?

  • LYYLatex Patient Examination Glove2decisions

What has FDA decided for it lately?

  • K893651Surgicare (R) Latex Examination GlovesInter Continental Health Care · 1989
  • K893756Surgicare (R) Specialty Examination GlovesInter Continental Health Care · 1989

All 2 as Inter Continental Health Care →

Other applicant names beginning “Inter”

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

Inter-Med, Inc. 12Inter-Med/Vista Dental Products 6Inter Medical Medizintechnik GmbH 3Inter Med Industries, Inc. 3Inter Science Institute 3Inter-Os Technologies 2Inter-Asia Co., Inc. 1Inter-Pal GmbH 1Inter-Med / Vista Dental 1Inter-Continental Industries Sdn Bhd 1