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

F-SERIES IMPLANT

K Number: K850706 · Decision Apr 10, 1985
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
12
Review Days
47

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Basic Information

Device Name
F-SERIES IMPLANT
K Number
K850706
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Omni Intl., Inc.
Date Received
February 22, 1985
Decision Date
April 10, 1985
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 Omni Intl., Inc.

K Number Device Name
K984066 OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIM
K984064 OMNIGRIP, LATEX SURGICAL GLOVE, POWDER FREE
K853255 OMNIMED I.V. SOLUTION ADMIN. SET
K851938 OMNIMED SURGICAL GOWN
K851654 OMNIMED CLAMP
K851734 OMNIMED SUPERIOR TRANSDUCER PROTECTOR
K850112 OMNIMED IV SOLUTION ADMINISTRATION SET
K850066 OMNIMED NASAL OXYGEN CANNULA
K831147 OMNIPROBE ELECTRICAL NERVE STIMULATOR
K821523 OMNI TENS
Search all 12 clearances from Omni Intl., Inc. →