Ecential Robotics

FDA Regulatory Profile

Ecential Robotics has 0 FDA recalls, 2 inspections, 7 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 12, 2026 · NAI
Latest 510(k)
Jul 22, 2026

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances7Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 12, 2026Gieres, FranceDevicesNo Action Indicated (NAI)3021060474
Jan 26, 2024Gieres, FranceDevicesVoluntary Action Indicated (VAI)3021060474

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3021060474Gieres, France2Jun 12, 2026

Recent 510(k) Clearances

K-NumberDeviceDate
K261113Op.n™ Spine Navigation and Robotic GuidanceJul 22, 2026
K242914Op.n(TM) NavigationMar 7, 2025
K233228Spine Navigation and Robotic-Assistance DeviceJun 14, 2024
K231886SURGIVISIO DeviceJul 27, 2023
K221028SURGIVISIO DeviceJul 6, 2022
K220946SURGIVISIO DeviceApr 15, 2022
K220627SURGIVISIO DeviceMar 18, 2022

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.