FDA Device Intelligence
Home › DX PRODUCTS LIMITED › Bathmate

Bathmate

DX PRODUCTS LIMITED · Model Hydromax 8 AB · UDI-DI 05060140201014

LKY
10
510(k) clearances
17
Adverse events
0
Recalls
48
Facilities

Description

Bathmate Hydromax 8 Aqua Blue

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 docs
Data 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.