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

MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER

K Number: K882063 · Decision Jun 13, 1988
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
23
Applicant Total
14
Review Days
28

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Basic Information

Device Name
MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER
K Number
K882063
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.3165
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Zest Anchors, Inc.
Date Received
May 16, 1988
Decision Date
June 13, 1988
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EGG), ordered by most recent decision date.

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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)
K925700 ZEST ANCHOR ADVANCED GENERATION
K861561 ZEST MARK II (STANDARD & MINI)
Search all 14 clearances from Zest Anchors, Inc. →