Home › Reshape Lifesciences Inc. › Model 2002 Maestro Rechargeable Neuroregulator

Model 2002 Maestro Rechargeable Neuroregulator

Reshape Lifesciences Inc. · Model 2002 · UDI-DI 00857334004262

PIM Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

The Model 2002 Rechargeable Neuroregulator (RNR) is provided sterile for implantation and has a hermetic case enclosure with an integrated coil that acts as an antenna for telemetry and recharging. The RNR is surgically implanted to deliver electrical current to the implanted leads. It contains a rechargeable battery which is charged transcutaneously using a Transmit Coil.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.