FDA applicant

Globalcare Intl., Inc.

Holyoke, MA4 decisions1991–19910 recalls

FDA records 4 decisions for Globalcare Intl., Inc. (Holyoke, MA) in 1991: 4 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and IPF (Stimulator, Muscle, Powered). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Globalcare Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Globalcare Intl., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Globalcare”

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

Globalcare Medical Technology Co., Ltd. 5 Globalcare/Bay Medical Corp. 1 Globalcare 1

Globalcare Intl., Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Globalcare”