FDA Device Intelligence
Home › Asp Global, LLC › JAMAR

JAMAR

Asp Global, LLC · Model 081656842 · UDI-DI 00840216112773

HRW
10
510(k) clearances
3
Adverse events
0
Recalls
47
Facilities

Description

JAMAR HAND EVALUATION KIT 2 WITH 30 LB PINCH GAUGE

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.