FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586

K Number: K033699 · Decision Apr 22, 2004
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
14
Review Days
149

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Basic Information

Device Name
LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586
K Number
K033699
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Zest Anchors, Inc.
Date Received
November 25, 2003
Decision Date
April 22, 2004
Product Code
DZE
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DZE Implant, Endosseous, Root-Form

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Other Clearances by Zest Anchors, Inc.

K Number Device Name
K150295 LOCATOR RTx
K083324 LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM
K072878 MODIFICATION TO: LOCATOR IMPLANT ANCHOR
K042466 X-2 IMPLANT ABUTMENT; BAR MALE; DISTAL EXTENSION MALE
K994257 LOCATOR IMPLANT ANCHOR
K925849 ZEST IMPLANT ANCHOR
K934668 ZEST IMPLANT ANCHOR ADVANCED GENERATION (DENTAL)
K925700 ZEST ANCHOR ADVANCED GENERATION
K882063 MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER
K861561 ZEST MARK II (STANDARD & MINI)
Search all 14 clearances from Zest Anchors, Inc. →