Reshape Lifesciences Inc.

6 devices · 66 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.

• Model 2002 Maestro Rechargeable Neuroregulator

  neuromodulator for obesity
  28 reports
• Model 2200P-47E Maestro Posterior Lead

  neuromodulator for obesity
  16 reports
• Model 2200A-47E Maestro Anterior Lead

  neuromodulator for obesity
  15 reports
• Model 2404 Maestro Patient Kit

  neuromodulator for obesity
  5 reports
• GIBI HD B-2032

  Tubes, Gastrointestinal (And Accessories)
  1 report
• GIBI HD B-2036

  Tubes, Gastrointestinal (And Accessories)
  1 report