Responsive Arthroscopy, LLC

FDA Regulatory Profile

Responsive Arthroscopy, LLC has 0 FDA recalls, 2 inspections, 13 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 30, 2024 · NAI
Latest 510(k)
Jul 20, 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) clearances13Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 30, 2024Minneapolis, MNDevicesNo Action Indicated (NAI)3015200759
Jan 30, 2020Minneapolis, MNDevicesNo Action Indicated (NAI)3015200759

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 3015200759Minneapolis, MN2May 30, 2024

Recent 510(k) Clearances

K-NumberDeviceDate
K261632Thunderbolt SystemJul 20, 2026
K253010Mini Superhawk Suture Anchor SystemOct 14, 2025
K243726Osprey Suture AnchorJan 30, 2025
K233258Shadow Knotless All-Suture AnchorsOct 23, 2023
K230094Responsive Arthroscopy Stealth and Mini Stealth All-Suture AnchorsAug 25, 2023
K222763Responsive Arthroscopy Mustang and Mustang Knotless Suture AnchorsOct 13, 2022
K203121Responsive Arthroscopy Thunderbolt SystemApr 27, 2021
K202569Responsive Arthroscopy Interference Screw SystemSep 23, 2020
K202153Responsive Arthroscopy Suture Anchor SystemSep 9, 2020
K190446Responsive Arthroscopy Wedge Push-In Suture AnchorsMar 27, 2019
K181076Responsive Arthroscopy Wedge Push-In Suture AnchorsJan 18, 2019
K180951Responsive Arthroscopy Suture Anchor SystemJan 3, 2019
K180573Responsive Arthroscopy Interference Screw SystemNov 23, 2018

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