FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
FIBER DISK AND BLOCK
K Number: K112186
·
Decision Nov 8, 2011
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
188
Applicant Total
3
Review Days
102
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Basic Information
- Device Name
- FIBER DISK AND BLOCK
- K Number
- K112186
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3770
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Bioloren S.R.L.
- Date Received
- July 29, 2011
- Decision Date
- November 8, 2011
- Product Code
- EBG
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| EBG | Crown And Bridge, Temporary, Resin | FDA class 2 | Dental |
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