FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ZEST ANCHOR ADVANCED GENERATION

K Number: K925700 · Decision Apr 7, 1994
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
23
Applicant Total
14
Review Days
511

Basic Information

Device Name
ZEST ANCHOR ADVANCED GENERATION
K Number
K925700
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.3165
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ZEST ANCHORS, INC.
Date Received
November 12, 1992
Decision Date
April 7, 1994
Product Code
EGG
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
EGG Attachment, Precision, All

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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
K925849 ZEST IMPLANT ANCHOR
K934668 ZEST IMPLANT ANCHOR ADVANCED GENERATION (DENTAL)
K882063 MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER
K861561 ZEST MARK II (STANDARD & MINI)
Search all 14 clearances from ZEST ANCHORS, INC. →