ROBODOC Surgical System receives FDA 510(k) marketing clearance
[REGULATORY ACTION]Jun 30, 2026 · ROBODOC · ROBODOC Surgical System · Sacramento, California, USA
Failure Mode
REGULATORY ACTION
Event Date
Jun 30, 2026
Primary Entity
ROBODOC
Robotic Platform
ROBODOC Surgical System
Jurisdiction / Location
Sacramento, California, USA
Audit Standard
Physical State Verified
Incident Abstract & Audit Findings
DigiMatch n ROBODOC Surgical System received FDA 510(k) marketing clearance for its orthopedic surgical robot platform.
System & Fleet Architecture
Operating Manufacturer
Hardware Platform
Operational Sectors
Primary Sources & Evidentiary Filings
- Inspect Filing
https://www.biospace.com/digimatch-tm-n-robodoc-surgical-system-receives-u-s-fda-510-k-marketing-clearance
https://www.biospace.com/digimatch-tm-n-robodoc-surgical-system-receives-u-s-fda-510-k-marketing-clearance
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Details
Incident Context & FAQ
What happened in ROBODOC Surgical System receives FDA 510(k) marketing clearance?
DigiMatch n ROBODOC Surgical System received FDA 510(k) marketing clearance for its orthopedic surgical robot platform.
When did this incident occur?
The incident is recorded as occurring on June 30, 2026 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.
What robot was involved in ROBODOC Surgical System receives FDA 510(k) marketing clearance?
ROBODOC Surgical System by ROBODOC is the recorded robot involved in this incident at Sacramento, California, USA.
Has anyone responded to ROBODOC Surgical System receives FDA 510(k) marketing clearance?
No responses to this incident are recorded on the DEPLOY registry. Operators, manufacturers, or affected parties can submit responses to the editorial team; absence is not a guarantee no response was issued.
What is the current status of ROBODOC Surgical System receives FDA 510(k) marketing clearance?
This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.