FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

PRIMOSPLINT SYSTEM

K Number: K030832 · Decision Sep 17, 2003
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
70
Applicant Total
28
Review Days
184

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Basic Information

Device Name
PRIMOSPLINT SYSTEM
K Number
K030832
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cosmedent, Inc.
Date Received
March 17, 2003
Decision Date
September 17, 2003
Product Code
MQC
Advisory Committee
Unknown
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
MQC Mouthguard, Prescription

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Other Clearances by Cosmedent, Inc.

K Number Device Name
K240714 Insure® Universal; Insure® Universal Automix
K222435 Renamel® Microhybrid ;Renamel® Flowable Microhybrid
K211259 Renamel Bulkfill
K172707 Renamel Microfill
K163480 Renamel NANO +plus
K092730 COSMEDENT BRUSHABLE COMPOSITE
K070583 NANO COMPOSITE
K060881 TEMPORARY CROWN & BRIDGE RESIN
K052263 MULTIPLE (TOOTH DESENSITIZER)
K052501 MULTIPLE RESIN TOOTH BONDING AGENT
Search all 28 clearances from Cosmedent, Inc. →