Lee-Alloy Disposable Capsules

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

510(k) Number

K780966 ↗

FDA Product Code

DZS

Device Class

Class I

Regulation

21 CFR Part 872.3110

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Precise(R) Beta Quartz Glass-Ceramic Insert

  Class II

  FDA 510(k) K912256 Active Cleared 24 Jul 1991

• Lee Endofill, Root Canal Filling Resin

  Class II

  FDA 510(k) K810923 Active Cleared 21 Apr 1981

• Ultraviolet Rad-Emitting Lamp

  Class II

  FDA 510(k) K771077 Active Cleared 24 Jun 1977

• Restobond 3/Dentin-Enamel Bonding Agent

  Class II

  FDA 510(k) K894315 Active Cleared 31 Oct 1989

• Cleanse N Bond I

  Class II

  FDA 510(k) K844133 Active Cleared 4 Jan 1985

• Restodent Vl

  Class II

  FDA 510(k) K843363 Active Cleared 25 Oct 1984

See all devices from Lee Pharmaceuticals →