510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K872215Substantially Equivalent

Perio-Test

Dr. Bernard Loewenthal, Portsmouth NH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K872215 is the FDA 510(k) clearance record for PERIO-TEST, a class I device, cleared for Dr. Bernard Loewenthal on under FDA product code EIL (Gauge, Depth, Instrument, Dental). FDA records list one 510(k) clearance for Dr. Bernard Loewenthal. As of , FDA records show no recalls naming K872215.

Clearance record

Decision date
Received
(31 days to decision)
Product code
EIL Gauge, Depth, Instrument, Dental
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
Dr. Bernard Loewenthal 278 Lafayette Rd., Portsmouth NH
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