Silimed Vaginal Stent

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K974479 ↗

FDA Product Code

KXP

Device Class

Class II

Regulation

21 CFR Part 884.3900

Advisory Committee

Obstetrics/Gynecology

FDA Decision

SESE Substantially Equivalent

• Silimed Nasal Retainer

  Class I

  FDA 510(k) K980221 Active Cleared 2 Apr 1998

• Silimed Calf Implant

  Class II

  FDA 510(k) K974480 Active Cleared 24 Feb 1998

• Silimed Gluteal Implant

  Class II

  FDA 510(k) K974482 Active Cleared 24 Feb 1998

• Silimed Pectoral Implant

  Class II

  FDA 510(k) K042054 Active Cleared 23 Feb 2005

• Silimed Nasal L Shaped Implant

  Class II

  FDA 510(k) K981833 Active Cleared 26 Jun 1998

• Silimed Silicone Carving Block

  Class II

  FDA 510(k) K981851 Active Cleared 9 Jul 1998

See all devices from Silimed, LLC →