510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K840855Substantially Equivalent

Corneal Scleral Lance

Sharpoint, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K840855 is the FDA 510(k) clearance record for CORNEAL SCLERAL LANCE, a class I device, cleared for Sharpoint, Inc. on under FDA product code HNN (Knife, Ophthalmic). FDA records list 9 510(k) clearances for Sharpoint, Inc., from to . As of , FDA records show no recalls naming K840855.

Clearance record

Decision date
Received
(75 days to decision)
Product code
HNN Knife, Ophthalmic
Regulation
21 CFR 886.4350
Device class
Class I
Review panel
Ophthalmic
Applicant
Sharpoint, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code HNN

Trailing 12 months

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

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