FDA Device Intelligence
HomeRobbins Instruments Inc. › Robbins Dermo-jet

Robbins Dermo-jet

Robbins Instruments Inc. · Model DJ-05 · UDI-DI 00199284222250

KZE
10
510(k) clearances
467
Adverse events (2 deaths)
1
Recalls
11
Facilities

Description

The Original Needle-Free Injection Device

Recalls

DateFirmReason
2010-06-01CaridianBCT, Inc.Labeling clarification and software updates to include fixes for end of run summaries, increasing boot reliability, corrections to the double red blood cell count collection TBV li

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.