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Unit, Electrosurgical, And Accessories, Dental
FDA product code EKZ · Class 2 · Dental
211
Registered devices
13
Adverse events
1
Recalls
19
510(k) clearances
Devices with this code
Macan — Macan ManufacturingMacan — Macan ManufacturingMacan — Macan ManufacturingMacan — Macan ManufacturingRoot ZX3 — J.MORITA MFG.CORP.Macan — Macan ManufacturingDento-Surg — Cynosure, LLCHenry Schein — HENRY SCHEIN, INC.Macan — Macan ManufacturingGT2 Small Loop Electrode — BONART CO., LTD.Macan — Macan ManufacturingNA — PARKELL, INC.Macan — Macan ManufacturingMacan — Macan ManufacturingMacan — Macan ManufacturingMacan — Macan ManufacturingMacan — Macan ManufacturingSensimatic® — PARKELL, INC.Macan — Macan ManufacturingMacan — Macan ManufacturingMacan — Macan ManufacturingE1 Hand Piece — BONART CO., LTD.Macan — Macan ManufacturingE1 Indiference Plate — BONART CO., LTD.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-04-05 | Macan Engineering and Manufacturing Co., Inc. | The product label fails to warn users to use the device on patients with shielded pacemakers only. |
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