Medical Device Manufacturer · US , Mchenry , IL

Almore Intl., Inc. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1980

Total

Cleared

Denied

Almore Intl., Inc. has 21 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 21 cleared submissions from 1980 to 1986.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Almore Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Almore Intl., Inc.

21 devices

1-12 of 21

Cleared Aug 12, 1986

ALMORE FACE MASK

K862851

General & Plastic Surgery · 14d

Cleared May 12, 1986

MONARCH II BLEACHING INSTRUMENT

K854692 · EEG

Dental · 172d

Cleared Mar 26, 1986

OP II VISIBLE LIGHT CURING SYSTEM

K854696 · EBZ

Dental · 125d

Cleared Mar 25, 1986

DIAMONDS BURS-COMPOSIT FINISHING

K854690 · EJL

Dental · 124d

Cleared Mar 25, 1986

DIAMOND BURS-HANDPIECE

K854691 · EJL

Dental · 124d

Cleared Mar 12, 1986

EZ-ON TUBING CONDITIONER (LUBRICANT)

K854700

Dental · 111d

Cleared Mar 06, 1986

TUBING HANDPIECE REPLACEMENT

PLASTIC MOUNTING RINGS

DOUBLE BOW TOOTH SEPARATOR

General & Plastic Surgery · 41d

Almore Intl., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Almore Intl., Inc.

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