QUANTEC-E ENDO SYSTEM— 510(k) K990739

Name: FDA 510(k) clearance K990739
Creator: U.S. Food and Drug Administration
Published: 1999-05-26

Substantially Equivalent

Sybron Dental Specialties, Inc.

FDA 510(k) clearance K990739 for QUANTEC-E ENDO SYSTEM, Substantially Equivalent on 1999-05-26. Applicant: Sybron Dental Specialties, Inc.. Device class: 1.

Clearance details

Applicant: Sybron Dental Specialties, Inc.
Product code: Code EKX
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 1999-03-05
Decision date: 1999-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orange, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EKX

view all

K261987 — Reusable SmartPeg2026-09-08
K252223 — Alpha Endo Handpiece (Alpha Endo)2025-10-16
K251597 — InnerView System2025-09-18
K243692 — EnDrive (EnDriveUS)2025-08-22
K242514 — Endo Motor (E-LITE MAX, E-LITE PRO, E-LITE INO)2025-04-24

More clearances from Sybron Dental Specialties, Inc.

view all

K093341 — CENTURY MODEL 105C2010-04-05
K091091 — SONICFILL 20102009-10-14
K080089 — SONICFLEX 2003 AND SONICFLEX LUX 2003 L WITH INSTRUMENT TIPS2008-09-04
K073478 — SUPERTORQUE HIGH-SPEED HANDPIECES AND GENTLEPOWER HANDPIECES AND ATTACHEMENTS2008-09-03
K071615 — FIXAFLOSS2007-09-21

Data sourced from openFDA. This site is unofficial and independent of the FDA.