510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K170520Substantially Equivalent

HyperVit Vitrectomy Probe, 23 GA, HyperVit Vitrectomy Probe, 25+, HyperVit Vitrectomy Probe, 27+

Alcon Laboratories, Lake Forest CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K170520 is the FDA 510(k) clearance record for HyperVit Vitrectomy Probe, 23 GA, HyperVit Vitrectomy Probe, 25+, HyperVit Vitrectomy Probe, 27+, a class II device, cleared for Alcon Research, Ltd. on under FDA product code MLZ (Vitrectomy, Instrument Cutter). FDA records list 152 510(k) clearances for Alcon Laboratories, from to . As of , FDA records show no recalls naming K170520.

Clearance record

Decision date
Received
(28 days to decision)
Product code
MLZ Vitrectomy, Instrument Cutter
Regulation
21 CFR 886.4150
Device class
Class II
Review panel
Ophthalmic
Applicant
Alcon Research, Ltd. 20511 Lake Forest Dr., Lake Forest CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MLZ

Trailing 12 months

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

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