Medtronic
Curved Suction 70 9733450 EM
1manufacturer
1catalogue number
Who Else Makes It
Registered in Guangdong.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Shenzhen Rainbow Technology Co., Ltd. | Shenzhen | Guangdong | Manufacturer | 12 |
Record
| Listed by | Medtronic Navigation, Inc., United States |
|---|---|
| FDA product code | HBC |
| Device type | Motor, Drill, Electric |
| Device class | Class 2 |
| Regulation | 21 CFR 882.4360 |
| Establishment | Specification developer, Repacker / relabeller, Manufacturer |
| 510(k) | K153555 |
| Record published | 2026-06-11 |
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 |
|---|---|---|
| 9733450 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| NSK Sterile Burs/Drills | Nakanishi Inc. | 447 |
| Motor, Drill, Electric | Anspach Effort, The | 168 |
| Primado2 | Nakanishi Inc. | 96 |
| Elan 4 | Aesculap AG | 39 |
| Midas REX® | Medtronic Powered Surgical Solutions | 29 |
| NSK Sterile Blades | Nakanishi Inc. | 24 |
| Motor, Drill, Electric | Synthes Gmbh | 22 |
| Aesculap | Aesculap AG | 14 |
| SSG10 | Saeshin Precision Co., Ltd. | 11 |
| Traus | Saeshin Precision Co., Ltd. | 9 |
| Midas Rex MR8 | Medtronic Powered Surgical Solutions | 7 |
| Eccos | Aesculap AG | 7 |
Showing 12 of 75. All products under Motor, Drill, Electric
Recalls Naming This Product
8 recalls name this product by its own identifiers, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Medtronic Navigation, Inc. | 510(k) number | 2017-06-29 | Class II | Device Design | The instruments are not able to pass instrument verification which is performed prior to the use of each instrument. | 277 instruments | 2018-08-03 |
| Medtronic Navigation, Inc. | 510(k) number | 2017-06-29 | Class II | Device Design | The instruments are not able to pass instrument verification which is performed prior to the use of each instrument. | 149 instruments | 2018-08-03 |
| Medtronic Navigation, Inc. | 510(k) number | 2017-06-29 | Class II | Device Design | The instruments are not able to pass instrument verification which is performed prior to the use of each instrument. | 75 instruments | 2018-08-03 |
| Medtronic Navigation, Inc. | 510(k) number | 2017-06-29 | Class II | Device Design | The instruments are not able to pass instrument verification which is performed prior to the use of each instrument. | 60 instruments | 2018-08-03 |
| Medtronic Navigation, Inc. | 510(k) number | 2017-06-29 | Class II | Device Design | The instruments are not able to pass instrument verification which is performed prior to the use of each instrument. | 13 kits | 2018-08-03 |
| Medtronic Navigation, Inc. | 510(k) number | 2017-06-29 | Class II | Device Design | The instruments are not able to pass instrument verification which is performed prior to the use of each instrument. | 15 kits | 2018-08-03 |
| Medtronic Navigation, Inc. | 510(k) number | 2017-06-29 | Class II | Device Design | The instruments are not able to pass instrument verification which is performed prior to the use of each instrument. | 8 kits | 2018-08-03 |
| Medtronic Navigation, Inc. | 510(k) number | 2017-06-29 | Class II | Device Design | The instruments are not able to pass instrument verification which is performed prior to the use of each instrument. | 6 kits | 2018-08-03 |
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.