510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K925395Substantially Equivalent

Technomed Pulsolith 4000 Laser System

Teknomed, Inc., Danvers MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925395 is the FDA 510(k) clearance record for TECHNOMED PULSOLITH 4000 LASER SYSTEM, a class II device, cleared for Teknomed, Inc. on under FDA product code LNK (Laser For Gastro-Urology Use). FDA records list 7 510(k) clearances for Teknomed, Inc., from to . As of , FDA records show no recalls naming K925395.

Clearance record

Decision date
Received
(207 days to decision)
Product code
LNK Laser For Gastro-Urology Use
Regulation
21 CFR 878.4810
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Teknomed, Inc. North Woods Business Park, Danvers MA
510(k) summary
Summary
Third party review
No

Clearances, product code LNK

Trailing 12 months

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

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