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Naslund Medical AB

FDA Regulatory Profile

Naslund Medical AB has 0 FDA recalls, 1 inspection, 4 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 3, 2023 · NAI
Latest 510(k)
Jan 6, 2022

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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) clearances4Oct 4, 2026Not statedCurrent
Inspections1Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
May 3, 2023Huddinge, SwedenDevicesNo Action Indicated (NAI)3008191247

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
K213053Gold AnchorJan 6, 2022
K201117Gold AnchorJun 11, 2020
K160209Gold AnchorJun 21, 2016
K091645GOLD ANCHORJul 21, 2009

FDA data resources