Home › NVision Biomedical Technologies, Inc. › nvc

nvc

NVision Biomedical Technologies, Inc. · Model AC-1214T-407 · UDI-DI 00814008022984

HTR

510(k) clearances

285

Adverse events (1 deaths)

Recalls

265

Facilities

Description

Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF)

Recalls

Date	Firm	Reason
2013-05-03	Surgical Instrument Service And Savings, Inc.	The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
2008-08-08	Sterilmed Inc	SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility e

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 key Read 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.