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Best Nomos

FDA Regulatory Profile

Best Nomos has 0 FDA recalls, 5 inspections, 5 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 11, 2018 · NAI
Latest 510(k)
May 6, 2021

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances5Oct 4, 2026Not statedCurrent
Inspections5Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 11, 2018Pittsburgh, PADevicesNo Action Indicated (NAI)2434141
Feb 3, 2016Pittsburgh, PADevicesNo Action Indicated (NAI)2434141
Oct 5, 2012Pittsburgh, PADevicesVoluntary Action Indicated (VAI)2434141
Oct 21, 2010Pittsburgh, PADevicesVoluntary Action Indicated (VAI)2434141
Jan 29, 2009Pittsburgh, PADevicesNo Action Indicated (NAI)2434141

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.

Recent 510(k) Clearances

K-NumberDeviceDate
K211034Corvus Radiation Therapy Planning SystemMay 6, 2021
K201350CORVUSSep 20, 2020
K170345SOFTDISOOct 27, 2017
K151469CORVUS Radiation Therapy Planning SystemNov 25, 2015
K100092CORVUS RADIATION THERAPY PLANNING SYSTEMFeb 23, 2010

FDA data resources