FDA Device Intelligence
Home › MIZUHO CORPORATION › Dual Needle Holder

Dual Needle Holder

MIZUHO CORPORATION · Model 07-861-14 · UDI-DI 04946329210231

HAO Prescription
10
510(k) clearances
351
Adverse events
2
Recalls
211
Facilities

Description

Dual Needle Holder Straight (For Deep Area)

Recalls

DateFirmReason
2011-04-04Zimmer Inc.A rounded or partially rounded tip on the screwdriver may not provide the required locking torque to lock the closure top to the polyaxial screw. When the hex tip of the screwdrive
2010-07-02Integra LifeSciences CorpCertain NeuroBalloon Catheters have the potential to improperly inflate or deflate under certain conditions.

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.