FDA applicant

Fischer Surgical, Inc.

Imperial, MO1 decision2012–20120 recalls

FDA records 1 decision for Fischer Surgical, Inc. (Imperial, MO) in 2012: 1 510(k) clearance. All are in product code OTZ (Graft Insertion Instrument For Endothelial…). 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, ophthalmic panel, where it files most

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

FDA decisions per year

1in 2012

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Fischer Surgical, Inc. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Fischer Surgical, Inc.’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 “Fischer”

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

Fischer Imaging Corp. 69 Fischer Industries, Inc. 3 Fischer-Zoth Audiologic Systems, Inc. 2 Fischer Medical 1 Fischer Medical Technologies, Inc. 1

Fischer Surgical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Fischer”