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

ZEST IMPLANT ANCHOR

K Number: K925849 · Decision Nov 18, 1994
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
14
Review Days
730

Basic Information

Device Name
ZEST IMPLANT ANCHOR
K Number
K925849
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 18, 1992
Decision Date
November 18, 1994
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
K033699 LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586
K994257 LOCATOR 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. →