510(k) Report

FDA applicant

Sds Dental, Inc.

Washington, DC21 decisions1986–19990 recalls

FDA records 21 decisions for Sds Dental, Inc. (Washington, DC) from 1986 to 1999: 21 510(k) clearances. Most are in product codes EIA (Unit, Operative Dental) and FSY (Light, Surgical, Ceiling Mounted). 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Sds Dental, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sds Dental, 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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