Home › Device types › LRY
Punch, Surgical
FDA product code LRY · Class 1 · General, Plastic Surgery
2,555
Registered devices
762
Adverse events
6
Recalls
7
510(k) clearances
Devices with this code
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbHAESCULAP — Aesculap AGAmbler Surgical — AMBLER SURGICAL CORP.Arthrex® — ARTHREX, INC.RZ Medizintechnik GmbH — RZ-Medizintechnik GmbHRZ Medizintechnik GmbH — RZ-Medizintechnik GmbH0.90 mm regular punch, 10 pack — Cole Instruments IncRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHAESCULAP — Aesculap AGRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHKerrison — RZ-Medizintechnik GmbHRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHTarget Endoscopic Instrument — SOLENDOS Inc.Henry Schein — HENRY SCHEIN, INC.Ambler Surgical — AMBLER SURGICAL CORP.ORTHOMED — ORTHO-MED, INC.Endo-Kerrison — Joimax GmbHNOIR — Aesculap AGHELMUT ZEPF — Helmut Zepf Medizintechnik GmbHRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHATTUNE — DEPUY (IRELAND)Ambler Surgical — AMBLER SURGICAL CORP.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-10-23 | Alto Development Corp | Surgical punches are being recalled due to potential packaging damage which may have occurred during transportation resulting in loss of sterility. |
| 2016-01-08 | DePuy Orthopaedics, Inc. | Increased punch height, causing a 0.063 in (1.6 mm) gap between the trial and the instrument. This may cause the surgeon to select an insert that is too thin. |
| 2013-03-18 | Clorox Healthcare Holdings, LLC (dba HealthLink) | Due to lack of sterilization. |
| 2013-03-18 | Clorox Healthcare Holdings, LLC (dba HealthLink) | Due to lack of sterilization. |
| 2013-03-18 | Clorox Healthcare Holdings, LLC (dba HealthLink) | Due to lack of sterilization. |
| 2012-08-14 | Biomet, Inc. | Investigation found that the current design of the product allows the press-fit of the knob/shaft interface to be overcome by the impaction force of a mallet, c |
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