Bivona Nasal Turbinate Stent

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K935053 ↗

FDA Product Code

LYA

Device Class

Class I

Regulation

21 CFR Part 874.4780

Advisory Committee

Ear, Nose, Throat

FDA Decision

SESE Substantially Equivalent

• Fome-Cuf-Wire Re-Enforced, Aire-Cuf Wire

  Class II

  FDA 510(k) K792035 Active Cleared 26 Oct 1979

• Aire-Cuf Polyester Re-Enforced Endotracheal Tube

  Class II

  FDA 510(k) K872366 Active Cleared 17 Aug 1987

• Fome-Cuf Pvc

  Class II

  FDA 510(k) K780583 Active Cleared 12 May 1978

• Fome-Cuf and Aire Cuf Tracheostomy Tubes

  Class II

  FDA 510(k) K862267 Active Cleared 18 Jun 1986

• Bivona Carden Intermittent Jetting Device

  Class II

  FDA 510(k) K895946 Active Cleared 9 Jan 1990

• Bivona Fome-Cuf(R) Pediatric Tracheostomy Tube

  Class II

  FDA 510(k) K913270 Active Cleared 9 Aug 1991

See all devices from Bivona Medical Technologies →