510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K945102Substantially Equivalent

Mta:angenieux Starpoint Xe Xenon Light Source

Alm Surgical Equipment, Inc., Anaheim CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K945102 is the FDA 510(k) clearance record for MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCE, a class II device, cleared for Alm Surgical Equipment, Inc. on under FDA product code FFS (Image, Illumination, Fiberoptic, For Endoscope). FDA records list 10 510(k) clearances for Alm Surgical Equipment, Inc., from to . As of , FDA records show no recalls naming K945102.

Clearance record

Decision date
Received
(17 days to decision)
Product code
FFS Image, Illumination, Fiberoptic, For Endoscope
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Alm Surgical Equipment, Inc. 1820 N. Lemon St., Anaheim CA
510(k) summary
Summary
Third party review
No

Clearances, product code FFS

Trailing 12 months

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

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