Physicians Choice Silicone Ear Putty

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

510(k) Number

K823921 ↗

FDA Product Code

LDG

Device Class

Class I

Regulation

21 CFR Part 874.3300

Advisory Committee

Ear, Nose, Throat

FDA Decision

SESE Substantially Equivalent

• Bores* Adjustable Blade Holder

  Class I

  FDA 510(k) K812070 Active Cleared 18 Aug 1981

• Rk IV Surgical Blades

  Class I

  FDA 510(k) K812071 Active Cleared 31 Aug 1981

• Otological Ventilation Tubes

  Class II

  FDA 510(k) K802638 Active Cleared 12 Nov 1980

• Medco Custom Ear Protector Mold Kit

  Unclassified

  FDA 510(k) K821187 Active Cleared 27 May 1982

• Nasal Septal Button

  Unclassified

  FDA 510(k) K850492 Active Cleared 7 Mar 1985

• Bores* Depth Gauge

  Class I

  FDA 510(k) K812069 Active Cleared 31 Aug 1981

See all devices from Santa Barbara Medco, Inc. →