PANAVIA V5: Standard Kit (Universal (A2)), Standard Kit (Clear), Introductory Kit (Universal (A2)), Introductory Kit (Clear), Sample Pack (Universal (A2)), Paste (Universal (A2)), Paste (Clear), Paste (Brown (A4)), Paste (White), Paste (Opaque), Try-in Paste (Universal (A2)), Try-in Paste (Clear), Try-in Paste (Brown (A4)), Try-in Paste (White), Try-in Paste (Opaque), Tooth Primer
K150704 is the FDA 510(k) clearance record for PANAVIA V5: Standard Kit (Universal (A2)), Standard Kit (Clear), Introductory Kit (Universal (A2)), Introductory Kit (Clear), Sample Pack (Universal (A2)), Paste (Universal (A2)), Paste (Clear), Paste (Brown (A4)), Paste (White), Paste (Opaque), Try-in Paste (Universal (A2)), Try-in Paste (Clear), Try-in Paste (Brown (A4)), Try-in Paste (White), Try-in Paste (Opaque), Tooth Primer, a class II device, cleared for Kuraray Noritake Dental, Inc. on under FDA product code EMA (Cement, Dental). FDA records list 32 510(k) clearances for Kuraray Noritake Dental, Inc., from to . As of , FDA records show no recalls naming K150704.
Clearance record
- Decision date
- Received
- (156 days to decision)
- Product code
- EMA Cement, Dental
- Regulation
- 21 CFR 872.3275
- Device class
- Class II
- Review panel
- Dental
- Applicant
- Kuraray Noritake Dental, Inc. Ote Center Bldg. 7f, 1-1-3, Otemachi, Chiyoda Ku, JP
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code EMA
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 3 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 1 |
| April 2026 | 1 |
| May 2026 | 1 |
| June 2026 | 0 |
| July 2026 | 1 |
| August 2026 | 2 |
| September 2026 | 1 |
| October 2026 | 0 |
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