510(k) Report

FDA applicant

Surgi-Aid Endoscopics, Inc.

Valencia, CA1 decision1987–19870 recalls

FDA records 1 decision for Surgi-Aid Endoscopics, Inc. (Valencia, CA) in 1987: 1 510(k) clearance. All are in product code OCZ (Endoscopic Grasping/Cutting Instrument…). 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 Surgi-Aid Endoscopics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Surgi-Aid Endoscopics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Surgi-Aid Endoscopics, 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 “Surgi-Aid”

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