K073106Substantially Equivalent
Unifast III
GC America Inc., Alsip IL / Traditional, Substantially Equivalent
K073106 is the FDA 510(k) clearance record for UNIFAST III, a class II device, cleared for GC America, Inc. on under FDA product code EBG (Crown And Bridge, Temporary, Resin). FDA records list 128 510(k) clearances for GC America, Inc., from to . As of , FDA records show no recalls naming K073106.
Clearance record
- Decision date
- Received
- (161 days to decision)
- Product code
- EBG Crown And Bridge, Temporary, Resin
- Regulation
- 21 CFR 872.3770
- Device class
- Class II
- Review panel
- Dental
- Applicant
- GC America, Inc. 3737 W. 127th St., Alsip IL
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code EBG
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 1 |
| April 2026 | 1 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
| November 2026 | 0 |
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