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Intraoperative Orthopedic Joint Assessment Aid
FDA product code ONN · Class 2 · Neurology
203
Registered devices
6
Adverse events
8
Recalls
18
510(k) clearances
Devices with this code
VERASENSE — ORTHOSENSOR INCVERASENSE — ORTHOSENSOR INCLinkstation MINI Evaluation Kit — ORTHOSENSOR INCVERASENSE — ORTHOSENSOR INCVERASENSE — ORTHOSENSOR INCVERASENSE — ORTHOSENSOR INCVERASENSE — ORTHOSENSOR INCLinkStation MINI Evaluation Kit — ORTHOSENSOR INCVERASENSE — ORTHOSENSOR INCVERASENSE — ORTHOSENSOR INCLantern Surgical Assistant — Orthalign, Inc.VERASENSE — ORTHOSENSOR INCLantern — Orthalign, Inc.VERASENSE — ORTHOSENSOR INCVERASENSE — ORTHOSENSOR INCVERASENSE — ORTHOSENSOR INCVERASENSE — ORTHOSENSOR INCVERASENSE — ORTHOSENSOR INCLinkStation MINI Evaluation Kit — ORTHOSENSOR INCLantern — Orthalign, Inc.VERASENSE — ORTHOSENSOR INCVERASENSE for Exactech Equinoxe Reverse — ORTHOSENSOR INCVERASENSE — ORTHOSENSOR INCVERASENSE — ORTHOSENSOR INC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-07-12 | Orthosensor, Inc. | Some sensors were reported to have fluid inside the posterior lateral corner post-surgery. |
| 2018-07-12 | Orthosensor, Inc. | Some sensors were reported to have fluid inside the posterior lateral corner post-surgery. |
| 2018-07-12 | Orthosensor, Inc. | Some sensors were reported to have fluid inside the posterior lateral corner post-surgery. |
| 2018-07-12 | Orthosensor, Inc. | Some sensors were reported to have fluid inside the posterior lateral corner post-surgery. |
| 2018-07-12 | Orthosensor, Inc. | Some sensors were reported to have fluid inside the posterior lateral corner post-surgery. |
| 2018-07-12 | Orthosensor, Inc. | Some sensors were reported to have fluid inside the posterior lateral corner post-surgery. |
| 2014-12-05 | Orthosensor, Inc. | Presence of one inoperable (dead) sensor pad. |
| 2012-02-04 | Orthosensor | Ortho sensor in Sunrise, FL is recalling the Graphics User Interface Software 1.8 (which was updated to version 1.82, validated on 02/13/12). Recall was initiat |
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