Home › Device types › HAM
Apparatus, Electrosurgical
FDA product code HAM · Class 2 · General, Plastic Surgery
54
Registered devices
72
Adverse events
3
Recalls
31
510(k) clearances
Devices with this code
Kirwan — KIRWAN SURGICAL PRODUCTS LLCABC — Conmed CorporationCONMED — Conmed CorporationABC — Conmed CorporationKirwan — KIRWAN SURGICAL PRODUCTS LLCPILLING — TELEFLEX INCORPORATEDKirwan — KIRWAN SURGICAL PRODUCTS LLCVivid Electrode Tip #2 — PEARSON DENTAL SUPPLIES, INC.Symmetry Olsen — ASPEN SURGICAL PRODUCTS, INC.ESI — FTT MEDICAL, INC.Symmetry Olsen — ASPEN SURGICAL PRODUCTS, INC.Vivid Surgo Matic — PEARSON DENTAL SUPPLIES, INC.Symmetry Olsen — ASPEN SURGICAL PRODUCTS, INC.Kirwan — KIRWAN SURGICAL PRODUCTS LLCKirwan — KIRWAN SURGICAL PRODUCTS LLCVivid Electrode Tip #21 — PEARSON DENTAL SUPPLIES, INC.WECK — TELEFLEX INCORPORATEDESI — FTT MEDICAL, INC.Vivid Electrode Tip #11 — PEARSON DENTAL SUPPLIES, INC.ITL Essential Standard Quiver — ITL ASIA PACIFIC SDN. BHD.Vivid Electrode Tip #14 — PEARSON DENTAL SUPPLIES, INC.Vivid Electrode Tip #1 — PEARSON DENTAL SUPPLIES, INC.ESI — FTT MEDICAL, INC.ITL Essential Laparoscopic Quiver Extendable — ITL ASIA PACIFIC SDN. BHD.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-12-27 | ConMed Corporation | ConMed received complaints of some devices which had broken through the seal of the sterile pouch. ConMed confirmed instances where the pouch seal was compromi |
| 2003-07-16 | Valleylab, Inc | Pads may have a thin plastic film covering the conductive gel surface underneath the normal printed cover, causing non-adherence and possible burn. |
| 2003-07-16 | Valleylab, Inc | Pads may have a thin plastic film covering the conductive gel surface underneath the normal printed cover, causing non-adherence and possible burn. |
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