Home › Device types › GDT
Staple, Removable (Skin)
FDA product code GDT · Class 1 · General, Plastic Surgery
104
Registered devices
4,743
Adverse events
5
Recalls
19
510(k) clearances
Devices with this code
microMend PRO — Kitotech Medical IncProximate — ETHICON ENDO-SURGERY, LLCmicroMend PRO — Kitotech Medical Inc3M™ Precise™ — 3M COMPANYWECK — TELEFLEX INCORPORATEDASP MEDICAL — Asp Global, LLCMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.3M™ Precise™ — 3M COMPANYCARDINAL HEALTH — Cardinal Health 200, LLCEthicon — ProvisionMichel Wound Clips — SONTEC INSTRUMENTS, INC.Appose ULC — Covidien LPBandGrip® Micro-Anchor® Skin Closure — BANDGRIP INC.Proximate — ETHICON ENDO-SURGERY, LLCBandGrip® Micro-Anchor® Skin Closure — BANDGRIP INC.microMend — Kitotech Medical IncmicroMend PRO — Kitotech Medical Inc3M™ Precise™ — 3M COMPANYMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.Proximate — ETHICON ENDO-SURGERY, LLCWECK — TELEFLEX INCORPORATEDmicroMend PRO — Kitotech Medical IncNA — Integra Lifesciences CorporationCARDINAL HEALTH — Cardinal Health 200, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-02-15 | Teleflex Medical | Some boxes are labeled as Visistat Wide devices, when in fact the contain Visistat Regular devices. The 6 individually packaged units within the boxes are corr |
| 2017-03-24 | Teleflex Medical | Some boxes are labeled as containing Visistat Wide devices, when they in fact they contained Visistat Regular device. |
| 2016-11-18 | Teleflex Medical | Sterility Deficiency: The packages are not sealed properly and thus the sterility is not assured. |
| 2015-07-10 | Customed, Inc | Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile. |
| 2014-10-08 | Customed, Inc | Customed products are being recalled because of compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing |
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