510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K936221Substantially Equivalent

Probe Tip/peri Probe/peri Probe Comp.

Pd International AB, Sloane, SE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K936221 is the FDA 510(k) clearance record for PROBE TIP/PERI PROBE/PERI PROBE COMP., a class I device, cleared for Pd International AB on under FDA product code EIX (Probe, Periodontic). FDA records list one 510(k) clearance for Pd International AB. As of , FDA records show no recalls naming K936221.

Clearance record

Decision date
Received
(217 days to decision)
Product code
EIX Probe, Periodontic
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
Pd International AB
510(k) summary
Statement
Third party review
No

Clearances, product code EIX

Trailing 12 months

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

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