Home › Device types › GDO
Applier, Surgical, Clip
FDA product code GDO · Class 1 · General, Plastic Surgery
1,428
Registered devices
16,547
Adverse events
8
Recalls
14
510(k) clearances
Devices with this code
WECK — TELEFLEX INCORPORATEDWECK — TELEFLEX INCORPORATEDWECK — TELEFLEX INCORPORATEDSurgical Direct — Surgical Direct, Inc.WECK — TELEFLEX INCORPORATEDBOSS Instruments — BOSS INSTRUMENTS, LTD., INC.WECK — TELEFLEX INCORPORATEDBOSS Instruments — BOSS INSTRUMENTS, LTD., INC.Novo Surgical Inc. — NOVO SURGICAL, INC.TELEFLEX — TELEFLEX INCORPORATEDLAZIC — Peter Lazic GmbHTELEFLEX — TELEFLEX INCORPORATEDWECK — TELEFLEX INCORPORATEDWECK — TELEFLEX INCORPORATEDSurgical Direct — Surgical Direct, Inc.WECK — TELEFLEX INCORPORATEDWECK — TELEFLEX INCORPORATEDWECK — TELEFLEX INCORPORATEDLIGACLIP — ETHICON ENDO-SURGERY, LLCWECK — TELEFLEX INCORPORATEDWECK — TELEFLEX INCORPORATEDWECK — TELEFLEX INCORPORATEDWECK — TELEFLEX INCORPORATEDAESCULAP — Aesculap AG
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-08-24 | Teleflex Medical | Misbranded: Incorrect etching on the device. |
| 2015-11-02 | The Anspach Effort, Inc. | Assembled with the incorrect (smaller) front clips (component 44-0495 instead of 44.0498). |
| 2013-04-12 | Ethicon Endo-Surgery Inc | Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP 10mm M/L Endoscopic Rotating Multiple Clip Applier (ER320) due to potential clip formation an |
| 2013-04-12 | Ethicon Endo-Surgery Inc | Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP 10mm M/L Endoscopic Rotating Multiple Clip Applier (ER320) due to potential clip formation an |
| 2013-04-12 | Ethicon Endo-Surgery Inc | Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP 10mm M/L Endoscopic Rotating Multiple Clip Applier (ER320) due to potential clip formation an |
| 2004-06-07 | Ethicon Endo-Surgery | This device is subject to recall due to an increased possibility of clip scissoring which can result in less than optimal clip formation which may or may not se |
| 2003-05-21 | Weck | Some stylets were not bent sufficiently during the packaging process to preclude them from sliding back into the cannula during shipment. |
| 2001-10-31 | Weck | The flush port on some appliers was occluded with an epoxy resin during manufacturing. |
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