MAUDE manufacturer profile
INTRINSIC THERAPEUTICS · QES
MAUDE profile for Reherniation Reduction Device
Key facts
| Manufacturer | INTRINSIC THERAPEUTICS |
|---|---|
| Manufacturer group | INTRINSIC THERAPEUTICS |
| Product code | QES |
| Product code name | Reherniation Reduction Device |
At a glance
- 100–999 MAUDE reports
- 10–99 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Adverse Event Without Identified Device or Use Problem, Hernia, Pain, Vertebral Fracture, Failure to Seal, Device Dislodged or Dislocated, Improper or Incorrect Procedure or Method, Limb Pain Most reported problems
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE manufacturer and product code profiles
Manufacturer profiles aggregate MAUDE reports for one manufacturer within one product code, the level at which device safety signals are usually reviewed.
Source: U.S. Food and Drug Administration (FDA), MAUDE database; aggregation by Orca1