FDA applicant

Research Endoscope Systems Intl.

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Research Endoscope Systems Intl. (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code FHN (Ligator, Hemorrhoidal). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Research Endoscope Systems Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Research Endoscope Systems Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Research”

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

Research Medical, Inc. 35 Research Instruments, Ltd. 9 Research Development Corp. 6 Research Industries Corp. 5 Research Diagnostics, Inc. 3 Research Consultants, Inc. 1 Research Surgical Systems 1 Research Instrumentation Associates, Inc. 1

Research Endoscope Systems Intl.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Research”