Home › Device types › MGO
Closure, Wound, Adhesive
FDA product code MGO · Class 1 · General, Plastic Surgery
17
Registered devices
3
Adverse events
9
Recalls
1
510(k) clearances
Devices with this code
Vitale — CELLERA LLCVitale — CELLERA LLCZeni Medical — Focus Health Group, Inc.Zeni Medical — Focus Health Group, Inc.T-STRIP — PRECISION MEDICAL DEVICES, LLCZeni Medical — Focus Health Group, Inc.Vitale — CELLERA LLCVitale — CELLERA LLCVitale — CELLERA LLCZeni Medical — Focus Health Group, Inc.Vitale — CELLERA LLCMEDLINE INDUSTRIES, INC. — MEDLINE INDUSTRIES, INC.Vitale — CELLERA LLCZeni Medical — Focus Health Group, Inc.Vitale — CELLERA LLCZeni Medical — Focus Health Group, Inc.Vitale — CELLERA LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
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