510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K062740Substantially Equivalent

Jindell High Spped Air Turbine Handpiece, Models Sw, Sp, Su, Etu, Mu

Jindell Medical Instruments Co., Ltd., Hsin-Chu City, TW / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K062740 is the FDA 510(k) clearance record for JINDELL HIGH SPPED AIR TURBINE HANDPIECE, MODELS SW, SP, SU, ETU, MU, a class I device, cleared for Jindell Medical Instruments Co., Ltd. on under FDA product code EFB (Handpiece, Air-Powered, Dental). FDA records list one 510(k) clearance for Jindell Medical Instruments Co., Ltd. As of , FDA records show no recalls naming K062740.

Clearance record

Decision date
Received
(50 days to decision)
Product code
EFB Handpiece, Air-Powered, Dental
Regulation
21 CFR 872.4200
Device class
Class I
Review panel
Dental
Applicant
Jindell Medical Instruments Co., Ltd. # 58, Fu-Chiun St., Hsin-Chu City, TW
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EFB

Trailing 12 months
4 clearances under product code EFB in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code EFB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20262
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20261