FDA Device Intelligence
HomeHoogland Spine Products GmbH › MaxMoreSpine

MaxMoreSpine

Hoogland Spine Products GmbH · Model 1001-HS 001 · UDI-DI 04260200313546

HRR
8
510(k) clearances
39
Adverse events
1
Recalls
183
Facilities

Description

Hook Scissors Forceps, l = 320 mm, 2.7 mm

Recalls

DateFirmReason
2023-05-12MEDLINE INDUSTRIES, LP - NorthfieldThe scissors were manufactured without a tip protector resulting in the scissors breaking through the semi-rigid plastic tray compromising sterility.

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.