510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K100414Substantially Equivalent

Protoe Endosorb Small Hammer Toe Pin

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

K100414 is the FDA 510(k) clearance record for PROTOE ENDOSORB SMALL HAMMER TOE PIN, a class II device, cleared for Merete Medical GmbH on under FDA product code JDW (Pin, Fixation, Threaded). FDA records list 27 510(k) clearances for MERETE GMBH, from to . As of , FDA records show no recalls naming K100414.

Clearance record

Decision date
Received
(136 days to decision)
Product code
JDW Pin, Fixation, Threaded
Regulation
21 CFR 888.3040
Device class
Class II
Review panel
Orthopedic
Applicant
Merete Medical GmbH Alt Lankwitz 102, Berlin, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JDW

Trailing 12 months
1 clearance under product code JDW in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JDW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260