Home › J & J INSTRUMENTS INC › J & J INSTRUMENTS
J & J INSTRUMENTS
J & J INSTRUMENTS INC · Model 55-2380 · UDI-DI 00817524028829
7
510(k) clearances
11
Adverse events
0
Recalls
165
Facilities
Description
LISTER SCI. 8.5"" FLOOR QUALIT
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.