FDA Device Intelligence
HomeNingbo Guangyuan Zhixin Biological Technology Co., Ltd. › SpinMedix® Absorbable Fibrous Membrane

SpinMedix® Absorbable Fibrous Membrane

Ningbo Guangyuan Zhixin Biological Technology Co., Ltd. · Model ZK-015 · UDI-DI 06975222391141

OWWFTL
1
510(k) clearances
3
Adverse events
3
Recalls
16
Facilities

Recalls

DateFirmReason
2026-02-06International Life SciencesAugmentation devices failed bacterial endotoxin testing.
2026-02-06International Life SciencesAugmentation devices failed bacterial endotoxin testing.
2026-02-06International Life SciencesAugmentation devices failed bacterial endotoxin testing.

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.