Home › Device types › EBW
Controller, Foot, Handpiece And Cord
FDA product code EBW · Class 1 · Dental
523
Registered devices
392
Adverse events
2
Recalls
61
510(k) clearances
Devices with this code
SET PROIMPLANT 3RD GEN CA 20:1 — Bien-Air Dental SAwoodpecker — Guilin Woodpecker Medical Instrument Co., Ltd.ELECTROmatic PM-S — KaVo Dental GmbHOsseoSet 300, SI-1015 — W & H Dentalwerk Bürmoos GmbHTRAUS SUS10 — Saeshin Precision Co., Ltd.SiroCam AF — SIRONA Dental Systems GmbHX-CUBE — Saeshin Precision Co., Ltd.CONSOLE BIOPOWER — Bien-Air Dental SASurgic Pro+ — NAKANISHI INC.ELECTROmatic M-S — KaVo Dental GmbHSM3 — HIOSSEN, INC.SPRAYVIT — SIRONA Dental Systems GmbHELECTROmatic C-S — KaVo Dental GmbHDongle SPI — W & H Dentalwerk Bürmoos GmbHMEDIDENTA — HANDPIECE PARTS & REPAIRS, INC.TRAUS SUS10 — Saeshin Precision Co., Ltd.Chiropro 980 4 Buttons Foot Control — Bien-Air Dental SACastellini — CEFLA SOCIETA' COOPERATIVAFoot Control S-NW CAN-Bus DSI — W & H Dentalwerk Bürmoos GmbHA-dec — A-DEC, INC.NLX — NAKANISHI INC.WI-75 E/KM 20:1 — W & H Dentalwerk Bürmoos GmbHTube Holder — NAKANISHI INC.SURGmatic S201 L Pro — KaVo Dental GmbH
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-12-21 | W & H DentalWerk Burmoos GMBH - Site 1 | During continuous postmarket surveillance activities, we have noticed a potential malfunction of individual foot controls of the type S-N1/S-N2. In case the err |
| 2013-10-24 | Nobel Biocare Usa Llc | The recall was initiated because there is a potential for malfunction of the OsseoCare Pro when used with the OseeoCare Pro iPad application software release 1. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
