DEPLOYDatabase

Deployment

Remanufactured da Vinci Xi EndoWrist Instruments at Germany, Europe

FDA 510(k)-cleared remanufactured da Vinci Xi robotic surgical instruments including Permanent Cautery Hook and Permanent Cautery Spatula. Cleared under K252926.

Remanufactured da Vinci Xi EndoWrist Instruments by Restore Robotics · Unverified · Surgical robots


Commercial product — available for purchase in this market.

Exposure

Customer segment
healthcare
Scale tier
commercial 10 99

Each exposure value carries its own basis marker. Aggregators report a number; this surface preserves the source class so verification depth travels with the value.

Safety record

1 incident on record (1 minor). Most recent: Mar 2026.

minor
1

Most recent: Mar 2026

Only active incidents are counted. Retracted incidents are excluded from this summary but remain reachable at their canonical URLs.

Incidents on record (1)

Direct incidents recorded against this deployment. Retracted incidents are excluded here but remain reachable at their canonical URLs.

Trust tier
Unverifiedhow tiers work →
Last updated
2026-08-20
Status
operational
Operator type
customer deployed
Scale at site
2 to 10 units
Site environment
indoor
Location precision
city centroid
First seen
2024-06-01
ID
2692b41c-1116-44b8-917d-047b0972a2a2

Timeline

  1. Jun 2024
    First recorded
    Remanufactured da Vinci Xi EndoWrist Instruments first documented operating at Germany, Europe.
  2. Aug 2026
    Current status: operational, reviewed
    Latest recorded state. New status transitions append here as the deployment-status recorder produces them.

On the deployment map

Operates worldwide

Remanufactured da Vinci Xi EndoWrist Instruments is deployed globally rather than at a single verified site, so there is no map pin.

Free to use on your site, with a link back to DEPLOY.

Remanufactured da Vinci Xi EndoWrist Instruments operates in Germany, Europe. Explore the full verified map:

Methodology: Claimed (not independently verified) · no sources on file · last reviewed 2026-08-20

Verification posture

Claimed (not independently verified)

Low confidence

Review state

Stable

Last reviewed 2026-08-20

Maturity + lifecycle

Maturity stage: commercial

Lifecycle: active

Architectural position

Cohort: surgical

The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.

Methodology surface for Remanufactured da Vinci Xi EndoWrist Instruments at Germany, Europe.

Common questions

What is the Remanufactured da Vinci Xi EndoWrist Instruments deployment at Germany, Europe?
Remanufactured da Vinci Xi EndoWrist Instruments, built by Restore Robotics, is recorded as a deployment at Germany, Europe on the DEPLOY registry. Restore Robotics operates the deployment directly.
Who operates Remanufactured da Vinci Xi EndoWrist Instruments at Germany, Europe?
Restore Robotics, the manufacturer of Remanufactured da Vinci Xi EndoWrist Instruments, operates this deployment directly. This is a maker-deploys-its-own-product arrangement rather than a customer pilot.
When did the Remanufactured da Vinci Xi EndoWrist Instruments deployment at Germany, Europe go live?
The deployment is recorded as starting June 1, 2024 on the DEPLOY registry. Earlier activity may exist but is not yet sourced.
Have there been incidents at the Remanufactured da Vinci Xi EndoWrist Instruments deployment at Germany, Europe?
1 active incident affecting this deployment is on the DEPLOY registry. Each is a sourced, append-only record; retracted incidents are suppressed from this view.
Is Remanufactured da Vinci Xi EndoWrist Instruments at Germany, Europe safe?
Remanufactured da Vinci Xi EndoWrist Instruments at Germany, Europe has 1 active incident on record in the DEPLOY registry. 1 incident on record (1 minor). Most recent: Mar 2026. Retracted incidents are excluded from this count.

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Machine-readable surfaces