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Henry Schein

HENRY SCHEIN, INC. · Model 5703110 · UDI-DI 00304040165201

EHK
8
510(k) clearances
3
Adverse events
1
Recalls
121
Facilities

Description

ESA Disp Prophy Angles LF MW Soft, 100/Bx

Recalls

DateFirmReason
2023-07-20Cosmedent, Inc.Reports were received the elastomer cup material is crumbling.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.