510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K072251Substantially Equivalent

Merete Toemobile Anatomical Great Toe Resurfacing System

Merete GmbH, Rye NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072251 is the FDA 510(k) clearance record for MERETE TOEMOBILE ANATOMICAL GREAT TOE RESURFACING SYSTEM, cleared for Merete Medical GmbH on under FDA product code LZJ (Prosthesis, Toe (Metatarsophalangeal), Joint, Metal/Polymer, Semi-Constrained). FDA records list 27 510(k) clearances for MERETE GMBH, from to . As of , FDA records show no recalls naming K072251.

Clearance record

Decision date
Received
(269 days to decision)
Product code
LZJ Prosthesis, Toe (Metatarsophalangeal), Joint, Metal/Polymer, Semi-Constrained
Device class
Unclassified
Review panel
Unknown
Applicant
Merete Medical GmbH 49 Purchase St., Rye NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LZJ

Trailing 12 months

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

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