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
K923711Substantially Equivalent

Perioflex Tip

Novadent, Ltd., Jerusalem, IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923711 is the FDA 510(k) clearance record for PERIOFLEX TIP, a class I device, cleared for Novadent, Ltd. on under FDA product code EFS (Unit, Oral Irrigation). FDA records list one 510(k) clearance for Novadent, Ltd. As of , FDA records show no recalls naming K923711.

Clearance record

Decision date
Received
(658 days to decision)
Product code
EFS Unit, Oral Irrigation
Regulation
21 CFR 872.6510
Device class
Class I
Review panel
Dental
Applicant
Novadent, Ltd. P.O. Box 45127, Jerusalem, IL
510(k) summary
Summary
Third party review
No

Clearances, product code EFS

Trailing 12 months

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

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