Home › Device types › GDT
Staple, Removable (Skin)
FDA product code GDT · Class 1 · General, Plastic Surgery
104
Registered devices
4,768
Adverse events
5
Recalls
19
510(k) clearances
Devices with this code
microMend PRO — Kitotech Medical IncmicroMend PRO — Kitotech Medical IncmicroMend — Kitotech Medical IncProximate — ETHICON ENDO-SURGERY, LLCTaiwan Surgical — TAIWAN SURGICAL CORPORATIONmicroMend PRO — Kitotech Medical IncAppose ULC — Covidien LPTrinity Sterile, Inc. — Trinity Sterile, Inc.NA — HARITEX CORPORATIONProximate — ETHICON ENDO-SURGERY, LLCWECK — TELEFLEX INCORPORATEDmicroMend PRO — Kitotech Medical IncMcKesson — MCKESSON MEDICAL-SURGICAL INC.ARROW — TELEFLEX INCORPORATEDEthicon — ProvisionMICHEL WOUND CLIPS — SONTEC INSTRUMENTS, INC.NA — Integra Lifesciences CorporationMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.3M™ Precise™ — 3M COMPANYASP MEDICAL — Asp Global, LLCmicroMend PRO — Kitotech Medical IncWECK — TELEFLEX INCORPORATEDAuto Suture — Covidien LPProximate — ETHICON ENDO-SURGERY, 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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