510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K955072Substantially Equivalent

Laminaria

Cti Corp., Ltd., Vacaville CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K955072 is the FDA 510(k) clearance record for LAMINARIA, a class II device, cleared for Cti Corp., Ltd. on under FDA product code HDY (Dilator, Cervical, Hygroscopic-Laminaria). FDA records list one 510(k) clearance for Cti Corp., Ltd. As of , FDA records show no recalls naming K955072.

Clearance record

Decision date
Received
(198 days to decision)
Product code
HDY Dilator, Cervical, Hygroscopic-Laminaria
Regulation
21 CFR 884.4260
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Cti Corp., Ltd. 607 Elmira Rd., Vacaville CA
510(k) summary
Statement
Third party review
No

Clearances, product code HDY

Trailing 12 months

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

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