Home › BENCO DENTAL SUPPLY CO. › BENCO
BENCO
BENCO DENTAL SUPPLY CO. · Model 4052-320 · UDI-DI 00366975019257
EFD
Prescription
10
510(k) clearances
6
Adverse events
1
Recalls
32
Facilities
Description
High Speed Amalgamator
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-20 | SDI Limited | Potential for electrical discharge from unit when unplugged. |
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 docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
