510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K101782Substantially Equivalent

Microstaar Msi Injector System Cartridge

Staar Japan, Monrovia CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K101782 is the FDA 510(k) clearance record for MICROSTAAR MSI INJECTOR SYSTEM CARTRIDGE, a class I device, cleared for Staar Japan on under FDA product code MSS (Folders And Injectors, Intraocular Lens (Iol)). FDA records list one 510(k) clearance for Staar Japan. As of , FDA records show no recalls naming K101782.

Clearance record

Decision date
Received
(180 days to decision)
Product code
MSS Folders And Injectors, Intraocular Lens (Iol)
Regulation
21 CFR 886.4300
Device class
Class I
Review panel
Ophthalmic
Applicant
Staar Japan 1911 Walker Ave., Monrovia CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MSS

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