510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K060995Substantially Equivalent

Duckworth & Kent Ltd Lens Delivery System, Model Dk7788

Duckworth & Kent, Ltd., Baldock, Hertfordshire, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K060995 is the FDA 510(k) clearance record for DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM, MODEL DK7788, a class I device, cleared for Duckworth & Kent, Ltd. on under FDA product code MSS (Folders And Injectors, Intraocular Lens (Iol)). FDA records list 6 510(k) clearances for Duckworth & Kent, Ltd., from to . As of , FDA records show no recalls naming K060995.

Clearance record

Decision date
Received
(41 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
Duckworth & Kent, Ltd. 7 Marquis Business Centre, Baldock, Hertfordshire, GB
510(k) summary
Statement
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