FDA Device Intelligence
Home › DILON TECHNOLOGIES FRANCE › COVAORTHO-NERVE

COVAORTHO-NERVE

DILON TECHNOLOGIES FRANCE · Model MCG 14 46 V · UDI-DI 03760193182040

JXI Prescription
1
510(k) clearances
174
Adverse events
4
Recalls
39
Facilities

Description

Collagen Guided Healing Membrane

Recalls

DateFirmReason
2023-03-27Baxter Healthcare CorporationThe product is brittle and potentially crumbling upon handling or when being removed from its package.
2020-02-07Integra LifeSciences Corp.Nonconforming product which was dispositioned for rejection was mistakenly released for commercial use.
2013-03-28Integra LifeSciences CorporationDue to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.
2013-03-28Integra LifeSciences CorporationDue to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.

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.