510(k) Report

FDA applicant

Schick Technologies, Inc.

Long Island City, NY13 decisions1994–20110 recalls

FDA records 13 decisions for Schick Technologies, Inc. (Long Island City, NY) from 1994 to 2011: 13 510(k) clearances. Most are in product codes MUH (System, X-Ray, Extraoral Source, Digital) and EAP (Unit, X-Ray, Intraoral). Its devices cite 16 predicates, 13 of them its own earlier devices. 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 Schick Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2007: 12009: 12011: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Schick Technologies, 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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