ESZ
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Tube, Shunt, Endolymphatic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 874.3820
- Medical specialty
- Ear, Nose, Throat
- Flags
- Implant
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| Record | Firm | Date | Builder |
|---|---|---|---|
| ENDOLYMPHATIC SAC TO MASTOID T-SHUNT (K974224) | Exmoor Plastics , Ltd. | 1998-01-27 | + Add |
| C-FLEX ENDOLYMPHATIC SHUNT (K952227) | Trebay Medical Corp. | 1995-06-16 | + Add |
| GIBSON ENDOLYMPHATIC SHUNT (K897049) | Hood Laboratories | 1990-03-16 | + Add |
| AUSTIN ENDOLYMPH DISPERSMENT SHUNT (K834094) | Treace Medical, Inc. | 1984-09-20 | + Add |
Track ESZ automatically
Every clearance here is in the API, with alerts when new ones post.