510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K142204Substantially Equivalent

Bioceptive Suction Cervical Retractor

Bioceptive, Inc., New Orleans LA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K142204 is the FDA 510(k) clearance record for Bioceptive Suction Cervical Retractor, a class II device, cleared for Bioceptive, Inc. on under FDA product code HDC (Tenaculum, Uterine). FDA records list one 510(k) clearance for Bioceptive, Inc. As of , FDA records show no recalls naming K142204.

Clearance record

Decision date
Received
(130 days to decision)
Product code
HDC Tenaculum, Uterine
Regulation
21 CFR 884.4530
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Bioceptive, Inc. New Orleans Bioinnovation Center, 1441 Canal St., Suite 228, New Orleans LA
510(k) summary
Statement
Third party review
No

Clearances, product code HDC

Trailing 12 months

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

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