510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932529Substantially Equivalent

Lightspeed Dental Hand Instrument

Lightspeed Endodontics, Houston TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932529 is the FDA 510(k) clearance record for LIGHTSPEED DENTAL HAND INSTRUMENT, a class I device, cleared for Lightspeed Endodontics on under FDA product code EKS (File, Pulp Canal, Endodontic). FDA records list one 510(k) clearance for Lightspeed Endodontics. As of , FDA records show no recalls naming K932529.

Clearance record

Decision date
Received
(163 days to decision)
Product code
EKS File, Pulp Canal, Endodontic
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
Lightspeed Endodontics 5832 Auden, Houston TX
510(k) summary
Statement
Third party review
No

Clearances, product code EKS

Trailing 12 months

FDA records hold no clearances under product code EKS in the trailing twelve months.

FDA records show no clearances under product code EKS in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EKS, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260