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
K890493Substantially Equivalent

Florida Probe Periodontal Probe

Florida Probe Corp., Gainesville FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890493 is the FDA 510(k) clearance record for FLORIDA PROBE PERIODONTAL PROBE, a class I device, cleared for Florida Probe Corp. on under FDA product code EIL (Gauge, Depth, Instrument, Dental). FDA records list 2 510(k) clearances for Florida Probe Corp., from to . As of , FDA records show no recalls naming K890493.

Clearance record

Decision date
Received
(41 days to decision)
Product code
EIL Gauge, Depth, Instrument, Dental
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
Florida Probe Corp. 1820 NE 23rd Ave., Gainesville FL
Third party review
No

Clearances, product code EIL

Trailing 12 months

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

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