510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K822740Substantially Equivalent

K30000 Dental Chair

Kaycor Intl., Ltd., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K822740 is the FDA 510(k) clearance record for K30000 DENTAL CHAIR, a class I device, cleared for Kaycor Intl., Ltd. on under FDA product code KLC (Chair, Dental, With Operative Unit). FDA records list 7 510(k) clearances for Kaycor Intl., Ltd., from to . As of , FDA records show no recalls naming K822740.

Clearance record

Decision date
Received
(19 days to decision)
Product code
KLC Chair, Dental, With Operative Unit
Regulation
21 CFR 872.6250
Device class
Class I
Review panel
Dental
Applicant
Kaycor Intl., Ltd. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KLC

Trailing 12 months

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

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