Home › LIMACORPORATE SPA › ArTT

ArTT

LIMACORPORATE SPA · Model 8421.15.085 · UDI-DI 08033390300360

OQG LPH Prescription

510(k) clearances

673

Adverse events

Recalls

119

Facilities

Description

Revision Bone Screw - Self-tapping; Dia.6.5mm/L.85mm

Recalls

Date	Firm	Reason
2023-06-16	Conformis, Inc.	30mm screws were labeled as 25mm screws.
2013-01-24	Stelkast Co	Firm was made aware of incidents relating to the difficulty of properly engaging and securing the Cross-Over 36mm liner into the Cross-Over shell.

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.