Impactor
50 catalogue numbers from 00-5851-097-11, listed by Zimmer, Inc., United States, under Impactor. 18 manufacturers in China are registered for this product code.
18manufacturers in China registered for this device type
50catalogue numbers in this listing
3recalls on this code
Who Else Makes It
Concentrated in Jiangsu (6), Shanghai (4), Shandong (2). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Zhejiang Biomet Medical Products Co., Ltd. | Jinhua | Zhejiang | Contract manufacturer | 74 |
| Apex (Guangzhou) Tools & Orthopedics Company | Guangzhou | Guangdong | Contract manufacturer | 62 |
| Paragon Medical Device (Changzhou) Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 53 |
| Canwell Medical Co., Ltd. | Jinhua | Zhejiang | Contract manufacturer | 42 |
| Xinhua Healthcare Industry Co., Limited | Zibo | Shandong | Contract manufacturer | 30 |
| Guangzhou Aquila Precise Tools Limited | Guangzhou | Guangdong | Contract manufacturer | 28 |
| B-ONE Medical (Suzhou) Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 23 |
| Shanghai Medical Instruments (Group) Ltd. Corp. | Shanghai | Shanghai | Contract manufacturer | 235 |
| Xinhua Surgical Instrument Co., Ltd. | Zibo | Shandong | Manufacturer | 222 |
| Zimmer (Shanghai) Medical International Trading Co., Ltd. | Shanghai | Shanghai | Exporter | 106 |
| MicroPort Orthopedics Global Supply Center Limited | Shanghai | Shanghai | Contract manufacturer | 82 |
| Medtronic (Changzhou) Medical Devices Technology Co., Ltd. | Changzhou | Jiangsu | Manufacturer | 53 |
Showing 12 of 18. All 18 manufacturers in China registered for Impactor
Record
| Listed by | Zimmer, Inc., United States |
|---|---|
| FDA product code | HWA |
| Device type | Impactor |
| Device class | Class 1 |
| Regulation | 21 CFR 888.4540 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter |
| Premarket notification | Exempt |
| Record published | 2016-07-25 |
| Record revised | 2023-05-03 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Sizes | Lumen/inner diameter 22 to 32 mm |
| Distribution end date | 2017-05-16 |
Catalogue Numbers
| Catalogue number | Size | Per pack | Status |
|---|---|---|---|
| 00-5851-097-11 | In distribution | ||
| 00-5983-092-03 | In distribution | ||
| 6270-58 | 58/60 mm | In distribution | |
| 5785-33 | In distribution | ||
| 00-5785-033-02 | 2 | In distribution | |
| 00-5851-074-00 | In distribution | ||
| 6270-54 | 54/56 mm | In distribution | |
| 9027-57 | In distribution | ||
| 5941-04 | In distribution | ||
| 31-8106-70 | In distribution | ||
| 5785-34 | In distribution | ||
| 00-5851-000-51 | In distribution | ||
| 5100-03-710 | In distribution | ||
| 5120-38 | 2 | In distribution | |
| 6270-66 | 66/68 mm | In distribution | |
| 00-5851-074-02 | In distribution | ||
| 6270-46 | 46/48 mm | In distribution | |
| 00-1336-038-00 | In distribution | ||
| 6270-74 | 74/76 mm | In distribution | |
| 31-8106-42 | In distribution | ||
| 5120-34 | In distribution | ||
| 31-8106-41 | In distribution | ||
| 00-5853-074-05 | In distribution | ||
| 31-8106-39 | In distribution | ||
| 6270-78 | 78/80 mm | In distribution | |
| 6270-70 | 70/72 mm | In distribution | |
| 5983-92 | In distribution | ||
| 00-5851-097-12 | In distribution | ||
| 6270-38 | 38/40 mm | In distribution | |
| 6270-42 | 42/44 mm | In distribution | |
| 31-8106-38 | In distribution | ||
| 9027-58 | In distribution | ||
| 9206-02-100 | In distribution | ||
| 00-5851-080-00 | In distribution | ||
| 6270-50 | 50/52 mm | In distribution | |
| 6270-62 | 62/64 mm | In distribution | |
| 9366-28-002 | Lumen/Inner Diameter 28 mm | Withdrawn | |
| 9366-26-001 | Lumen/Inner Diameter 26 mm | Withdrawn | |
| 9366-22-000 | Lumen/Inner Diameter 22 mm | Withdrawn | |
| 9366-32-013 | 32 mm Insert Chamfer Impactor | Withdrawn | |
| 9366-22-008 | 22 mm Insert Rim Impactor | Withdrawn | |
| 9366-44-005 | 44 mm I.D. Insert Impactor | Withdrawn | |
| 9375-00-031 | Withdrawn | ||
| 9366-44-014 | 44 mm Insert Chamfer Impactor | Withdrawn | |
| 9206-02-005 | Withdrawn | ||
| 9366-32-003 | Lumen/Inner Diameter 32 mm | Withdrawn | |
| 9366-26-009 | 26 mm Insert Rim Impactor | Withdrawn | |
| 31-8106-82 | Withdrawn | ||
| 9366-28-010 | 28 mm Insert Rim Impactor | Withdrawn | |
| 31-8106-84 | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| R3 | Smith & Nephew, Inc. | 153 |
| Conserve® | Microport Orthopedics Inc. | 76 |
| DJO Surgical | Encore Medical, L.P. | 73 |
| Impactor | Synthes Gmbh | 56 |
| Innomed, Inc. | Innomed, Inc. | 53 |
| Impactor | Zimmer Trabecular Metal Technology, Inc. | 43 |
| iNSitu™ Hip System | Nextstep Arthropedix | 41 |
| Apex Knee System | Omni Life Science, Inc. | 40 |
| DJO Surgical | DJO, LLC | 36 |
| Evolution® | Microport Orthopedics Inc. | 35 |
| Medtronic Reusable Instruments | Medtronic Sofamor Danek, Inc. | 35 |
| Attune | Depuy (Ireland) | 31 |
Showing 12 of 825. All products under Impactor
Recalls
2 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 |
|---|---|---|---|---|---|
| 2014-10-14 | Class II | Labeling design | To provide clarifying instructions relating to the assembly/disassembly of the Trabecular Metal Tibial Impactor with/from TM tibial Impactor Pads due to complaints regarding Tibal Impactor pad fracture. | 4961 units | 2015-06-09 |
| 2014-10-14 | Class II | Labeling design | To provide clarifying instructions relating to the assembly/disassembly of the Trabecular Metal Tibial Impactor with/from TM tibial Impactor Pads due to complaints regarding Tibal Impactor pad fracture. | 1165 units | 2015-06-09 |
| 2008-06-30 | Not classified | Device Design | The instrument may fracture during use, resulting in metal fragments being left in the patient post-surgery, which could cause implant failure. | 1439 | 2009-11-12 |
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.