FDA applicant

Schott Fiber Optics, Inc.

Southbridge, MA2 decisions1989–19900 recalls

FDA records 2 decisions for Schott Fiber Optics, Inc. (Southbridge, MA) from 1989 to 1990: 2 510(k) clearances. Most are in product codes HIH (Hysteroscope (And Accessories)) and FAM (Sigmoidoscope And Accessories, Flexible/Rigid). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Schott Fiber Optics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Schott Fiber Optics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Schott”

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

Schott North America 1

Schott Fiber Optics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Schott”