Home › Device types › LRY
Punch, Surgical
FDA product code LRY · Class 1 · General, Plastic Surgery
2,523
Registered devices
756
Adverse events
6
Recalls
7
510(k) clearances
Devices with this code
Ambler Surgical — AMBLER SURGICAL CORP.ORTHOMED — ORTHO-MED, INC.Tornier Perform — TORNIER, INC.RZ Medizintechnik GmbH — RZ-Medizintechnik GmbHAESCULAP — Aesculap AGYEOMAN BIOSPY PUNCH RONGEUR — SONTEC INSTRUMENTS, INC.LAZIC — Peter Lazic GmbHAmbler Surgical — AMBLER SURGICAL CORP.1.15 mm Zero-T punch — Cole Instruments IncORTHOMED — ORTHO-MED, INC.RZ Medizintechnik GmbH — RZ-Medizintechnik GmbHNA — Synthes GmbHAmbler Surgical — AMBLER SURGICAL CORP.Ambler Surgical — AMBLER SURGICAL CORP.RZ Medizintechnik GmbH — RZ-Medizintechnik GmbHAmbler Surgical — AMBLER SURGICAL CORP.NOIR — Aesculap AGRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHMaxMoreSpine — Hoogland Spine Products GmbHRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHKerrison — RZ-Medizintechnik GmbHRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHRZ Medizintechnik GmbH — RZ-Medizintechnik GmbH
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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