510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K041621Substantially Equivalent

Liteport Lp100 Surgical Illuminator

Medical Vision Industries, Inc., Pleasant Hill CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K041621 is the FDA 510(k) clearance record for LITEPORT LP100 SURGICAL ILLUMINATOR, a class II device, cleared for Medical Vision Industries, Inc. on under FDA product code FTF (Illuminator, Non-Remote). FDA records list one 510(k) clearance for Medical Vision Industries, Inc. As of , FDA records show no recalls naming K041621.

Clearance record

Decision date
Received
(89 days to decision)
Product code
FTF Illuminator, Non-Remote
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Medical Vision Industries, Inc. 200 Gregory Ln. Suite C-100, Pleasant Hill CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FTF

Trailing 12 months

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

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