510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K151298Substantially Equivalent

Gemini XXP-HP

Dornier Medtech America, Inc., Kennesaw GA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K151298 is the FDA 510(k) clearance record for Gemini XXP-HP, a class II device, cleared for Dornier Medtech America on under FDA product code LNS (Lithotriptor, Extracorporeal Shock-Wave, Urological). FDA records list 46 510(k) clearances for Dornier Medtech America, from to . As of , FDA records show no recalls naming K151298.

Clearance record

Decision date
Received
(76 days to decision)
Product code
LNS Lithotriptor, Extracorporeal Shock-Wave, Urological
Regulation
21 CFR 876.5990
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Dornier Medtech America 1155 Roberts Blvd., Kennesaw GA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LNS

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