MAUDE manufacturer profile
ACCLARENT, INC. · LRC
MAUDE profile for Instrument, Ent Manual Surgical
Key facts
| Manufacturer | ACCLARENT, INC. |
|---|---|
| Manufacturer group | ACCLARENT, INC. |
| Product code | LRC |
| Product code name | Instrument, Ent Manual Surgical |
At a glance
- 100–999 MAUDE reports
- 1–9 Death reports
- 10–99 Injury reports
- 100–999 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- No Clinical Signs, Symptoms or Conditions, No Consequences Or Impact To Patient, Adverse Event Without Identified Device or Use Problem, Contamination of Device Ingredient or Reagent, Incorrect Interpretation of Signal, Detachment of Device or Device Component, Cerebrospinal Fluid Leakage, No Known Impact Or Consequence To Patient 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