FDA Device Intelligence
HomeKOROS U.S.A., INC. › Cervical SL5 Micro Curette Set

Cervical SL5 Micro Curette Set

KOROS U.S.A., INC. · Model 7420-00 · UDI-DI 10840199543776

FZS Prescription
10
510(k) clearances
71
Adverse events (1 deaths)
3
Recalls
219
Facilities

Description

Cervical SL5 Micro Curette Set Consists of the Following: 1 x 7420-80, 4 x 7420-60, 1 x 7420-50, 1 x 7420-40, 1 x 7420-30, 1 x 7420-20, 1 x 7420-10, 1 x 7422-60, 1 x 7422-50, 1 x 7422-40, 1 x 7422-30, 1 x 7424-20, 1 x 7424-10 & 1 x 7420-90

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.
2013-11-05Zimmer, Inc.Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged pr
2011-07-15X Spine Systems IncThe firm learned that the Torque Driver Handles were not actuating at a proper torque. It was determined that the handles were speed determinant and could output a higher torque i

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.