510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K811113Substantially Equivalent

Riess-Luhr

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

K811113 is the FDA 510(k) clearance record for RIESS-LUHR, a class I device, cleared for Allomedic on under FDA product code DZA (Drill, Dental, Intraoral). FDA records list one 510(k) clearance for Allomedic. As of , FDA records show no recalls naming K811113.

Clearance record

Decision date
Received
(54 days to decision)
Product code
DZA Drill, Dental, Intraoral
Regulation
21 CFR 872.4130
Device class
Class I
Review panel
Dental
Applicant
Allomedic 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DZA

Trailing 12 months

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

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