Rebound Therapeutics Corporation
2 devices · 2 adverse event reports · 0 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- AURORA® Surgiscope® AS8/130ANTISERA, ALL GROUPS, STREPTOCOCCUS SPP.1 report
- AURORA® AEC12F/100Electrosurgical, Cutting & Coagulation & Accessories1 report