FDA Device Intelligence
Home › GRI Medical & Electronic Technology Co., Ltd. › Invenio

Invenio

GRI Medical & Electronic Technology Co., Ltd. · Model TUF021 · UDI-DI 16931918144559

POZ
0
510(k) clearances
3
Adverse events
1
Recalls
13
Facilities

Description

Biopsy Pack_Sterile_8EA/CS

Recalls

DateFirmReason
2026-04-21ARROW INTERNATIONAL, LLCLidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo

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.