Medtronic
Short Curved Suction 90 9733451 EM
2manufacturers in China registered for this device type
1catalogue number
Who Else Makes It
Concentrated in Shanghai (1), Guangdong (1).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Jabil Circuit (Shanghai) Ltd. | Shanghai | Shanghai | Contract manufacturer | 31 |
| Guangdong Jinme Medical Technology Co., Ltd. | Foshan | Guangdong | Manufacturer | 13 |
Record
| Listed by | Medtronic Navigation, Inc., United States |
|---|---|
| FDA product code | ERL |
| Device type | Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece |
| Device class | Class 2 |
| Regulation | 21 CFR 874.4250 |
| 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 |
|---|---|---|
| 9733451 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| ENT MR8 | Medtronic Powered Surgical Solutions | 234 |
| Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece | Anspach Effort, The | 214 |
| Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece | Karl Storz GmbH & Co. KG | 208 |
| Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece | Synthes Gmbh | 126 |
| Midas Rex | Medtronic Powered Surgical Solutions | 97 |
| Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece | Stryker GmbH | 87 |
| Midas REX Microsaws | Medtronic Powered Surgical Solutions | 75 |
| Piezomed Pro Accessory | W&H Dentalwerk Bürmoos GmbH | 50 |
| Midas Rex Clearview™ | Medtronic Xomed, Inc. | 47 |
| Zethon | Zethon Ltd | 39 |
| NSK Sterile Burs/Drills | Nakanishi Inc. | 34 |
| Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece | Medtronic Xomed, Inc. | 29 |
Showing 12 of 169. All products under Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
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.