Provide®
USE-Provide® Abutment Analog 4.8MM(P) - 5.5MM Post
70manufacturers in China registered for this device type
6catalogue numbers in this listing
14recalls on this code
Who Else Makes It
Concentrated in Guangdong (28), Jiangsu (9), Zhejiang (6). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Shenzhen Denco Medical Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 52 |
| LX Precision Shanghai Co Ltd | Shanghai | Shanghai | Contract manufacturer | 19 |
| iBrite Suzhou Technology Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 18 |
| Digital Dental Depot | Zhuhai | Guangdong | Contract manufacturer | 17 |
| Xiamen Yizhou IMP. & EXP. Co., Ltd. | Xiamen | Fujian | Contract manufacturer | 10 |
| Amedcon Medical Technology (Shenzhen) Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 7 |
| Ningbo Sezen Technology Co., Ltd. | Ningbo | Zhejiang | Contract manufacturer | 7 |
| Boen Healthcare Co., Ltd. | Suzhou | Jiangsu | Specification developer | 263 |
| Debo Medical Technology (Shijiazhuang) Co., Ltd. | Shijiazhuang | Hebei | Contract manufacturer | 117 |
| Shanghai Jolly Industrial Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 99 |
| Shanghai Lions Industrial Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 82 |
| Wuxi Lyusmile IMP AND EXP Co., Ltd. | Wuxi | Jiangsu | Private-label distributor | 66 |
Showing 12 of 70. All 70 manufacturers in China registered for Accessories, Implant, Dental, Endosseous
Record
| Listed by | ZimVie US Corp LLC, United States |
|---|---|
| FDA product code | NDP |
| Device type | Accessories, Implant, Dental, Endosseous |
| Device class | Class 1 |
| Regulation | 21 CFR 872.3980 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| Premarket notification | Exempt |
| Record published | 2016-03-24 |
| Record revised | 2026-01-15 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Label carries | lot or batch number |
| Sizes | Height 4 to 5.5 mm |
| Distribution end date | 2016-08-10 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| PAA654 | Height 4 mm | In distribution |
| PAA485 | Height 5.5 mm | In distribution |
| PAAP65 | In distribution | |
| PAA484 | Height 4 mm | Withdrawn |
| PAAP48 | Withdrawn | |
| PAA655 | Height 5.5 mm | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Accessories, Implant, Dental, Endosseous | Southern Implants (PTY) Ltd | 1,379 |
| Accessories, Implant, Dental, Endosseous | Institut Straumann AG | 1,320 |
| Neobiotech Implant System | Neobiotech Co., Ltd. | 1,112 |
| Inclusive | Prismatik Dentalcraft, Inc. | 1,045 |
| Medentika | Medentika GmbH | 1,042 |
| BioHorizons | Biohorizons Implant Systems Inc. | 1,008 |
| IPD | Implant Protesis Dental 2004 SL | 998 |
| Klockner | Soadco, S.L. | 995 |
| Dynamic Abutment Solutions | Talladium España, SL | 877 |
| Neodent | Jjgc Indústria e Comércio de Materiais Dentários S.A. | 738 |
| Nobel Biocare® | Nobel Biocare AB | 703 |
| MIS | MIS Implants Technologies Ltd. | 615 |
Showing 12 of 7,548. All products under Accessories, Implant, Dental, Endosseous
Recalls
14 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2017-10-11 | Class II | Employee error | The device may contain a manufacturing condition affecting the geometry of the driver’s hex feature which prevents it from properly engaging the fixture mount transfer and/or a dental implant. | 356 units | 2019-03-13 |
| 2017-10-11 | Class II | Employee error | The device may contain a manufacturing condition affecting the geometry of the driver’s hex feature which prevents it from properly engaging the fixture mount transfer and/or a dental implant. | 891 kits | 2019-03-13 |
| 2017-10-11 | Class II | Employee error | The device may contain a manufacturing condition affecting the geometry of the driver’s hex feature which prevents it from properly engaging the fixture mount transfer and/or a dental implant. | 166 kits | 2019-03-13 |
| 2017-10-11 | Class II | Employee error | The device may contain a manufacturing condition affecting the geometry of the driver’s hex feature which prevents it from properly engaging the fixture mount transfer and/or a dental implant. | 30 kits | 2019-03-13 |
| 2017-07-10 | Class II | Under Investigation by firm | Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard IFUs. All the products were missing supplemental IFUs. | 76 products | 2019-08-05 |
| 2017-07-10 | Class II | Under Investigation by firm | Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard IFUs. All the products were missing supplemental IFUs. | 86 products | 2019-08-05 |
| 2017-07-10 | Class II | Under Investigation by firm | Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard IFUs. All the products were missing supplemental IFUs. | 423 products | 2019-08-05 |
| 2017-07-10 | Class II | Under Investigation by firm | Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard IFUs. All the products were missing supplemental IFUs. | 349 products | 2019-08-05 |
| 2015-11-16 | Class II | Software design (manufacturing process) | Images contained within radiographic transparency ART 1036 are undersized. | 686 | 2016-12-14 |
| 2015-09-21 | Class II | Process control | Inadequate biocompatibility testing. | 30,111 devices. | 2016-10-12 |
| 2015-09-21 | Class II | Process control | Inadequate biocompatibility testing. | 30,111 devices. | 2016-10-12 |
| 2015-08-10 | Class II | Labeling mix-ups | RASQ3N, a square, abutment screw driver tip has been labeled and distributed as RASH3N, a hexed, abutment screw driver tip. Additionally, the RASQ3N received the RASH3N’s laser marking “RASH3N” during manufacturing. | 103 pieces | 2016-10-12 |
| 2015-08-10 | Class II | Labeling mix-ups | The RASH3N, a hexed, abutment screw driver tip has been labeled and distributed as RASQ3N, a square, abutment screw driver tip. Additionally, the RASQ3N received the RASH3N’s laser marking “RASH3N” during manufacturing. | 96 pieces | 2016-10-12 |
| 2015-01-22 | Class II | Device Design | The Gemlock Long Hex Driver may not fit into the Fixture Mount Transfer (FMT) or the internal hex of the implant. | 627 units | 2015-08-03 |
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.