FDA applicant

Medivision Scope Service Center, Inc.

Anaheim, CA5 decisions1997–19990 recalls

FDA records 5 decisions for Medivision Scope Service Center, Inc. (Anaheim, CA) from 1997 to 1999: 5 510(k) clearances. Most are in product codes HRX (Arthroscope) and EOB (Nasopharyngoscope (Flexible Or 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, gastroenterology and urology panel, where it files most

How often FDA has decided Medivision Scope Service Center, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medivision Scope Service Center, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medivision Scope Service Center, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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See the 510(k) Report

Other applicant names beginning “Medivision”

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

Medivision Medical Imaging, Ltd. 4 Medivision Endoscopy 1 Medivision (U.S.A.), Inc. 1

Medivision Scope Service Center, Inc.

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 “Medivision”