510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K801969Substantially Equivalent

Asnis Guided Screw Systems

Howmedica Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K801969 is the FDA 510(k) clearance record for ASNIS GUIDED SCREW SYSTEMS, a class I device, cleared for Howmedica Corp. on under FDA product code HNC (Specula, Ophthalmic). FDA records list 409 510(k) clearances for Howmedica Corp., from to . As of , FDA records show no recalls naming K801969.

Clearance record

Decision date
Received
(8 days to decision)
Product code
HNC Specula, Ophthalmic
Regulation
21 CFR 886.4350
Device class
Class I
Review panel
Ophthalmic
Applicant
Howmedica Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HNC

Trailing 12 months

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

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