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

BIOCERAM ZEST PLANT

K Number: K840244 · Decision May 1, 1984
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
14
Review Days
102

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
BIOCERAM ZEST PLANT
K Number
K840244
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Zest Anchors, Inc.
Date Received
January 20, 1984
Decision Date
May 1, 1984
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

Similar 510(k) Clearances

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

View all

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
K882063 MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER
Search all 14 clearances from Zest Anchors, Inc. →