510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K052271Substantially Equivalent

Rinsendo

Air Techniques, Inc., Hicksville NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K052271 is the FDA 510(k) clearance record for RINSENDO, a class I device, cleared for Air Techniques, Inc. on under FDA product code NYL (Handpiece, Air-Powered, Root Canal Irrigation). FDA's definition for product code NYL reads: "To clean the root canal prior to filling and used for root canal irrigation". FDA records list 18 510(k) clearances for Air Techniques, Inc., from to . As of , FDA records show no recalls naming K052271.

Clearance record

Decision date
Received
(280 days to decision)
Product code
NYL Handpiece, Air-Powered, Root Canal Irrigation
Regulation
21 CFR 872.4200
Device class
Class I
Review panel
Dental
Applicant
Air Techniques, Inc. 70 Cantiague Rock Rd., Hicksville NY
510(k) summary
Statement
Third party review
No

Clearances, product code NYL

Trailing 12 months

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

FDA records show no clearances under product code NYL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NYL, 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