PermaSoft®
Contains one (1) 30 gram PermaSoft Powder Pink (N815001), one (1) 30 milliliter PermaSoft Liquid (N814001), and one (1) 15 milliliter PermaSoft Sealer (N811300). Items are not sold…
Contains one (1) 30 gram PermaSoft Powder Pink (N815001), one (1) 30 milliliter PermaSoft Liquid (N814001), and one (1) 15 milliliter PermaSoft Sealer (N811300). Items are not sold individually.
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 |
| Record published | 2017-01-31 |
| Record revised | 2022-05-06 (version 6) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Single use | Yes |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date, manufacturing date |
| Sizes | Weight 30 to 500 g; total volume 30 to 500 ml |
| Distribution end date | 2022-05-05 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| Powder Pink | Weight 500 g | Withdrawn |
| Powder Clear | Weight 30 g | Withdrawn |
| Trial Kit | Withdrawn | |
| Soft Denture Liner 500 G Kit Pink | Withdrawn | |
| Powder Pink | Weight 60 g | Withdrawn |
| Soft Denture Liner 120 G Kit Pink | Withdrawn | |
| Powder Clear | Weight 60 g | Withdrawn |
| Powder Clear | Weight 120 g | Withdrawn |
| Soft Denture Liner 120 G Kit Clear | Withdrawn | |
| Sealer | Total Volume 105 ml | Withdrawn |
| Powder Pink | Weight 120 g | Withdrawn |
| Soft Denture Liner 60 G Kit Clear | Withdrawn | |
| Liquid | Total Volume 60 ml | Withdrawn |
| Powder Clear | Weight 500 g | Withdrawn |
| Liquid | Total Volume 500 ml | Withdrawn |
| Soft Denture Liner 60 G Kit Pink | Withdrawn | |
| Promotional Pack | Withdrawn | |
| Soft Denture Liner Combination Kit | Withdrawn | |
| Sealer | Total Volume 30 ml | 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.