FDA Device Intelligence
Home › PREMIER DENTAL PRODUCTS COMPANY › Premier Cavity Prep

Premier Cavity Prep

PREMIER DENTAL PRODUCTS COMPANY · Model 1003228 · UDI-DI 00348783008296

EKC Prescription
2
510(k) clearances
7
Adverse events
8
Recalls
121
Facilities

Description

BLACK CUTTING INSTR 61/62

Recalls

DateFirmReason
2008-11-14Sybron Dental SpecialtiesThe tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed.
2008-11-14Sybron Dental SpecialtiesThe tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed.
2008-11-14Sybron Dental SpecialtiesThe tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed.
2008-11-14Sybron Dental SpecialtiesThe tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed.
2008-11-14Sybron Dental SpecialtiesThe tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed.
2008-11-14Sybron Dental SpecialtiesThe tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed.
2008-11-14Sybron Dental SpecialtiesThe tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed.
2008-11-14Sybron Dental SpecialtiesThe tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed.

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.