510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K020407Substantially Equivalent

Lorenz Blue Device

Biomet Microfixation, Jacksonville FL / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K020407 is the FDA 510(k) clearance record for LORENZ BLUE DEVICE, a class II device, cleared for Walter Lorenz Surgical, Inc. on under FDA product code MQN (External Mandibular Fixator And/Or Distractor). FDA records list 86 510(k) clearances for BIOMET MICROFIXATION, from to . As of , FDA records show no recalls naming K020407.

Clearance record

Decision date
Received
(16 days to decision)
Product code
MQN External Mandibular Fixator And/Or Distractor
Regulation
21 CFR 872.4760
Device class
Class II
Review panel
Dental
Applicant
Walter Lorenz Surgical, Inc. 1520 Tradeport Dr., Jacksonville FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MQN

Trailing 12 months

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

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