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

SUPERIOR ENDOSSEOUS DENTAL IMPLANT SYSTEM

K Number: K884732 · Decision May 18, 1989
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
17
Review Days
189

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Basic Information

Device Name
SUPERIOR ENDOSSEOUS DENTAL IMPLANT SYSTEM
K Number
K884732
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Bio-Interfaces, Inc.
Date Received
November 10, 1988
Decision Date
May 18, 1989
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 Bio-Interfaces, Inc.

K Number Device Name
K960164 BIO-INTERFACES, INC., BIORESORBABLE CALCIUM PHOSPHATE PARTICLES - BII-GRAFT 6140
K954763 BIO-INTERFACES, INC,. BII-PLAST
K950598 BIORESORBABLE CALCIUM PHOSPHATE PARTICLES - BLL-GRAFT
K950567 BIO-APATITE 6140 HA PARTICLES
K950511 BLL-FIL 6140 PARTICLES
K934049 BII-PORE(TM) CANAL WALL PROSTHESIS
K933688 BII-PORE
K941431 BONE GRAFT DELIVERY SYRINGES
K934430 BON APATITE HA PARTICLES
K934947 BII-PLAST
Search all 17 clearances from Bio-Interfaces, Inc. →