Almore Intl., Inc.
Almore Intl., Inc. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1986.
Top product codes for Almore Intl., Inc.
Recent clearances by Almore Intl., Inc.
- K862851 — ALMORE FACE MASK
- K854692 — MONARCH II BLEACHING INSTRUMENT
- K854696 — OP II VISIBLE LIGHT CURING SYSTEM
- K854690 — DIAMONDS BURS-COMPOSIT FINISHING
- K854691 — DIAMOND BURS-HANDPIECE
- K854700 — EZ-ON TUBING CONDITIONER (LUBRICANT)
- K854697 — TUBING HANDPIECE REPLACEMENT
- K854701 — RETRACT-A-CORD
- K854702 — PLASTIC MOUNTING RINGS
- K854699 — TUBING SYRING
- K831136 — DOUBLE BOW TOOTH SEPARATOR
- K831137 — STRAIGHT 5 HEMOSTAT
- K831138 — CURVED HEMOSTAT 5
- K830773 — MARKLEY THREADED WIRE
- K830775 — FACEBOW FOR BALANCE ARTICULATOR
- K830776 — MICROFIL CONTOURING INSTRUMENTS
- K830774 — BINOCULAR MAGNIFIER 2X
- K830777 — ELECTRIC MOUTH MIRROR
- K830878 — BINOCULAR LOUPE
- K811075 — BALANCE ARTICULATOR
- K801463 — OJ-1 ENDODONIC ROOT CANAL FILE HOLDER
Data sourced from openFDA. This site is unofficial and independent of the FDA.