Medical Device Manufacturer · US , Walker , MI

Zest Anchors, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1980

Total

Cleared

Denied

Zest Anchors, Inc. has 14 FDA 510(k) cleared dental devices. Based in Walker, US.

Historical record: 14 cleared submissions from 1980 to 2015.

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

Zest Anchors, Inc. is one of 5082 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Zest Anchors, Inc.

14 devices

1-14 of 14

LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM

K083324 · NHA

Dental · 105d

Cleared Dec 03, 2007

MODIFICATION TO: LOCATOR IMPLANT ANCHOR

LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE,...

K033699 · DZE

Dental · 149d

Cleared Mar 17, 2000

LOCATOR IMPLANT ANCHOR

ZEST IMPLANT ANCHOR ADVANCED GENERATION (DENTAL)

K934668 · DZE

Dental · 266d

Cleared Apr 07, 1994

ZEST ANCHOR ADVANCED GENERATION

K925700 · EGG

Dental · 511d

Cleared Jun 13, 1988

MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER

K882063 · EGG

Dental · 28d

Cleared May 21, 1986

ZEST MARK II (STANDARD & MINI)

ZEST ENDODONTIC STABILIZER

K801525 · ELS

Dental · 20d

Zest Anchors, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Zest Anchors, Inc.

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