FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ALLOYBOND
K Number: K981383
·
Decision Jun 16, 1998
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
21
Review Days
61
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Basic Information
- Device Name
- ALLOYBOND
- K Number
- K981383
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3200
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Southern Dental Industries, Inc.
- Date Received
- April 16, 1998
- Decision Date
- June 16, 1998
- Product Code
- KLE
- 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 |
|---|---|---|---|
| KLE | Agent, Tooth Bonding, Resin | FDA class 2 | Dental |
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Other Clearances by Southern Dental Industries, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K062065 | RIVA LUTING PLUS | Nov 15, 2006 | Substantially Equivalent |
| K062064 | RIVA BOND LC | Nov 9, 2006 | Substantially Equivalent |
| K050871 | RIVA PROTECT | Jun 10, 2005 | Substantially Equivalent |
| K050870 | RIVA LIGHT CURE | Jun 3, 2005 | Substantially Equivalent |
| K050331 | ADHESIVE 1 | Mar 24, 2005 | Substantially Equivalent |
| K042452 | RIVA SILVER | Dec 7, 2004 | Substantially Equivalent |
| K040393 | RIVA LUTING | Apr 30, 2004 | Substantially Equivalent |
| K032152 | BENCO ADMIX | Aug 6, 2003 | Substantially Equivalent |
| K031658 | BENCO SPHERICAL | Jul 29, 2003 | Substantially Equivalent |
| K030568 | RADII | Apr 24, 2003 | Substantially Equivalent |