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

Flexible Partial Resin

K Number: K250302 · Decision Jun 25, 2025
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
57
Review Days
142

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Basic Information

Device Name
Flexible Partial Resin
K Number
K250302
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Prismatik Dentalcraft, Inc.
Date Received
February 3, 2025
Decision Date
June 25, 2025
Product Code
EBI
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
EBI Resin, Denture, Relining, Repairing, Rebasing

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