FDA applicant

Accurate Surgical Instruments Co.

Toronto Canado M5v 1y9, CA9 decisions1981–19950 recalls

FDA records 9 decisions for Accurate Surgical Instruments Co. (Toronto Canado M5v 1y9, CA) from 1981 to 1995: 9 510(k) clearances. Most are in product codes FJS (Catheter, Peritoneal, Long-Term Indwelling) and FKX (System, Peritoneal, Automatic Delivery). 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 Accurate Surgical Instruments Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Accurate Surgical Instruments Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Accurate Surgical Instruments Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Accurate Surgical Instruments Co.’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 “Accurate”

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

Accurate Medical Therapeutics, Ltd. 4 Accurate Meditech, Inc. 2 Accurate Medical Devices, Inc. 1 Accurate Access, LLC 1

Accurate Surgical Instruments Co.

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 “Accurate”