Hy-Pro Lucitone®
Fibered Light. Contains four (4) 630 gram bottles of Hy-Pro Lucitone Powder and three (3) 430 milliliter bottles of Lucitone Liquid.
14manufacturers in China registered for this device type
20catalogue numbers in this listing
18510(k) clearances naming this product code
Who Else Makes It
Concentrated in Guangdong (6), Zhejiang (2), Hebei (1).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Aidite (Qinhuangdao) Technology Co., Ltd. | Qinhuangdao | Hebei | Repacker / relabeller | 17 |
| Shandong Huge Dental Material Corporation | Rizhao | Shandong | Manufacturer | 17 |
| Shen FU Arts LAB | Shen Zhen | Guangdong | Manufacturer | 15 |
| Liaoning Upcera Co., Ltd. | Benxi | Liaoning | Contract manufacturer | 10 |
| Shenzhen Upcera Digital Dental Technology Co., Ltd. | Shenzhen | Guangdong | Exporter | 10 |
| Riton 3D Technology Co., Ltd. | Guangzhou | Guangdong | Repacker / relabeller | 9 |
| Yamahachi Dental Material (Changshu) Co., Ltd. | Changshu | Jiangsu | Manufacturer | 9 |
| Guangzhou Heygears Imc.inc | Guangzhou | Guangdong | Specification developer | 8 |
| Hangzhou SHINING3D Dental Technology Co., Ltd. | Hangzhou | Zhejiang | Manufacturer | 7 |
| Ningbo Sezen Technology Co., Ltd. | Ningbo | Zhejiang | Contract manufacturer | 7 |
| Hunan Vsmile Biotechnology Co., Ltd. | Changsha | Hunan | Contract manufacturer | 6 |
| Shenzhen Piocreat 3D Technology Co., Ltd. | Shenzhen | Guangdong | Manufacturer | 6 |
Showing 12 of 14. All 14 manufacturers in China registered for Resin, Denture, Relining, Repairing, Rebasing
Record
| Listed by | Dentsply LLC, United States |
|---|---|
| FDA product code | EBI |
| Device type | Resin, Denture, Relining, Repairing, Rebasing |
| Device class | Class 2 |
| Regulation | 21 CFR 872.3760 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| Premarket notification | Exempt |
| Record published | 2017-02-10 |
| Record revised | 2022-05-06 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date, manufacturing date |
| Sizes | Weight 231 to 630 g; total volume 120 to 430 ml; weight 25 lb |
| Distribution end date | 2022-05-05 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 11-Unit Package | Total Volume 120 ml | Withdrawn |
| 540-Unit Powder | Weight 25 lb | Withdrawn |
| 11-Unit Package | Weight 231 g | Withdrawn |
| 11-Unit Package | Weight 231 g | Withdrawn |
| Denture Base Powder | Weight 231 g | Withdrawn |
| 120-Unit Package | Weight 630 g | Withdrawn |
| 540-Unit Powder | Weight 25 lb | Withdrawn |
| Denture Base Powder | Weight 231 g | Withdrawn |
| 120-Unit Package | Total Volume 430 ml | Withdrawn |
| Denture Base Powder | Weight 231 g | Withdrawn |
| 120-Unit Package | Total Volume 430 ml | Withdrawn |
| 540-Unit Powder | Weight 25 lb | Withdrawn |
| Denture Base Powder | Weight 231 g | Withdrawn |
| 30-Unit Powder | Weight 630 g | Withdrawn |
| 540-Unit Powder | Weight 25 lb | Withdrawn |
| 120-Unit Package | Total Volume 430 ml | Withdrawn |
| 30-Unit Powder | Weight 630 g | Withdrawn |
| 30-Unit Powder | Weight 630 g | Withdrawn |
| 11-Unit Package | Total Volume 120 ml | Withdrawn |
| 30-Unit Powder | Weight 630 g | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Vertex-Dental BV | Vertex-Dental B.V. | 760 |
| HI-I® | Fricke International, Inc. | 490 |
| Vitacrilic® | Fricke International, Inc. | 249 |
| Nature-Cryl® | GC America Inc. | 205 |
| Nobilium | Cmp Industries, LLC | 167 |
| Hygenic | Coltene/Whaledent Gmbh & Co. KG | 152 |
| AvaDent | Global Dental Science | 150 |
| Dentorium | Wright Medical Technology, Inc. | 137 |
| Duracetal | The Myerson Company Limited | 136 |
| RE-Fine Bright | Yamahachi Dental MFG. Co. | 134 |
| Axcent Acrylics | Garreco, LLC | 132 |
| Unbreakable by TCS | Thermoplastic Comfort SYS | 96 |
Showing 12 of 3,288. All products under Resin, Denture, Relining, Repairing, Rebasing
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K072713 | 2007-10-12 |
| K061580 | 2006-07-28 |
| K032892 | 2003-09-26 |
| K011560 | 2001-07-12 |
| K992956 | 1999-10-06 |
| K972573 | 1997-09-16 |
| K964040 | 1996-12-06 |
| K952351 | 1995-07-07 |
| K926406 | 1993-03-31 |
| K905702 | 1991-04-29 |
| K895742 | 1989-12-18 |
| K882482 | 1988-08-12 |
| K863324 | 1986-09-05 |
| K834409 | 1984-02-27 |
| K831647 | 1983-06-30 |
| K800400 | 1980-03-12 |
| K792042 | 1979-11-30 |
| K780786 | 1978-06-14 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.