LRE
- Product code
- LRE
- Device name
- Instrument, Prosthesis Modification For Ossicular Replacement Surgery, Sterile
- Device class
- Class 1
- 21 CFR
- 21 CFR 874.3540
- Medical specialty
- Ear, Nose, Throat
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: LRE
Classification and pathway per current FDA publications. Data from openFDA (CC0).