Longevity V-Lign®
2 catalogue numbers from 9501-46-01, listed by Zimmer, Inc., United States, under Burr, Orthopedic. 3 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Shanghai (1), Shandong (1), Beijing (1).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Shanghai Medical Instruments (Group) Ltd. Corp. | Shanghai | Shanghai | Contract manufacturer | 235 |
| Xinhua Surgical Instrument Co., Ltd. | Zibo | Shandong | Manufacturer | 222 |
| Beijing Fule Science & Technology Development Co., Ltd. | Beijing | Beijing | Manufacturer | 31 |
Record
| Listed by | Zimmer, Inc., United States |
|---|---|
| FDA product code | HTT |
| Device type | Burr, Orthopedic |
| Device class | Class 1 |
| Regulation | 21 CFR 888.4540 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter |
| Premarket notification | Exempt |
| Record published | 2017-01-27 |
| Record revised | 2018-03-29 (version 2) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Prescription | Prescription only |
| Label carries | lot or batch number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 9501-46-01 | In distribution | |
| 9501-46 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Imedicom High Speed Blade | Imedicom Co., Ltd. | 275 |
| Brasseler USA | Provision | 261 |
| Stryker | Provision | 243 |
| MicroAire | Provision | 238 |
| Conmed/Linvatec | Provision | 87 |
| Burr, Orthopedic | Jota AG | 64 |
| gSource | Gsource, LLC. | 54 |
| Brasseler | Provision | 13 |
| Percutaneous Foot Burrs, Arthodesis Burrs | GM DOS Reis Industria E Comercio Ltda | 13 |
| Aesculap | Aesculap AG | 11 |
| Medtronic | Provision | 10 |
| Arthrex | Provision | 8 |
Showing 12 of 117. All products under Burr, Orthopedic
Recalls
1 of these is 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 |
|---|---|---|---|---|---|
| 2017-05-11 | Class II | Nonconforming Material/Component | the devices used a different raw material to produce two countersink products which has higher hardness and higher carbon content resulting in device damage. | 138 (OUS 297) | 2017-11-03 |
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.