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HomeVERSAH, LLC › 2.0mm ZGO Tapered Pilot Drill 65mm length

2.0mm ZGO Tapered Pilot Drill 65mm length

VERSAH, LLC · Model ZPLTT-65 · UDI-DI 00850017652736

EJL Prescription
10
510(k) clearances
523
Adverse events
13
Recalls
267
Facilities

Description

ZGO Tapered Pilot Drills are used to create the initial hole in bone to prepare an osteotomy for zygomatic implant placement and monitor the drilling depth.

Recalls

DateFirmReason
2025-02-27Premier Dental Products CoThe hardness not meeting the material specification and may cause the diamond bur to bend.
2024-01-11Brasseler USA I LpThe device has a grip detail (right angle latch) out of specification causing the bur to not adequately latch in the handpiece.
2020-10-20Coltene Whaledent IncThe FG 557 bur was incorrectly packaged as the FG 57 bur. The FG 557 burs will remove more material than the FG 57 burs.
2020-10-20Coltene Whaledent IncThe FG 557 bur was incorrectly packaged as the FG 57 bur. The FG 557 burs will remove more material than the FG 57 burs.
2020-10-20Coltene Whaledent IncThe FG 557 bur was incorrectly packaged as the FG 57 bur. The FG 557 burs will remove more material than the FG 57 burs.
2020-10-20Coltene Whaledent IncThe FG 557 bur was incorrectly packaged as the FG 57 bur. The FG 557 burs will remove more material than the FG 57 burs.
2020-10-20Coltene Whaledent IncThe FG 557 bur was incorrectly packaged as the FG 57 bur. The FG 557 burs will remove more material than the FG 57 burs.
2020-07-15Hager & Meisinger GmbhUS-dates between the product package label and the bar code display.
2019-12-23Jjgc Industria E Comercio De Materials Dentarios SaThe laser engraving of the product incorrectly identifies the 4.3 Tapered Guided Surgery Drill as the "4.3+ Tapered Guided Surgery Drill".
2019-07-19Coltene /Whaledent AGA single batch of Diatech Diamond dental burs, 856-016-7-F, Round end taper, contain diamond burs with the same grit size (fine) and shape (round end taper) but different length.

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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.