FDA Device Intelligence
Home › Cerenovus, Inc. › TRUFILL

TRUFILL

Cerenovus, Inc. · Model 631-500 · UDI-DI 10886704029151

KGGSGU Prescription
0
510(k) clearances
99
Adverse events (7 deaths)
2
Recalls
5
Facilities

Description

Contents:one 1 g tube n-BCA with self-piercing luer cap one 1 g vial Ta Powder one 10 mL vial Ethiodized Oil

Recalls

DateFirmReason
2013-10-11Codman & Shurtleff, Inc.Incorrect instructions for use (IFU).
2013-10-11Codman & Shurtleff, Inc.Incorrect instructions for use (IFU).

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.