510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K855137Substantially Equivalent

Curity Fiberoptic Intubating Airway

The Kendal Co., Boston MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K855137 is the FDA 510(k) clearance record for CURITY FIBEROPTIC INTUBATING AIRWAY, a class I device, cleared for The Kendal Co. on under FDA product code CAE (Airway, Oropharyngeal, Anesthesiology). FDA records list 63 510(k) clearances for The Kendal Co., from to . As of , FDA records show no recalls naming K855137.

Clearance record

Decision date
Received
(78 days to decision)
Product code
CAE Airway, Oropharyngeal, Anesthesiology
Regulation
21 CFR 868.5110
Device class
Class I
Review panel
Anesthesiology
Applicant
The Kendal Co. One Federal St., Boston MA
Third party review
No

Clearances, product code CAE

Trailing 12 months

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

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