21 results · 13ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Rejuvenate Modular Stems Stryker Ireland Carrigtwohill Industrial Estate Carrigtwohill County Cork, Ireland Rejuvenate Modular Necks Stryker Howmedica Osteonics Corp. Mahwah, NJ 07430. Stem Bodies Rejuvenate Modular consists of 6 modular stems bodies in sizes 7-12. The Modular Stem bodies are made of TMZF alloy, developed specifically for orthopaedic applications. Rejuvenate Modular Necks The Rejuvenate Modular Necks are made of Cobalt Chrome. The necks in this system consist of 4 lengths in 4 mm increments. They are 30 mm, 34 mm, 38 mm and 42 mm. They come in multiple neck angles and versions in each length. They are 127, 130 and 132. The versions are 0, 8, 16 degrees. In total there are 16 unique neck implants in the Rejuvenate Modular System.

FDA Enforcement
Class II ·Ongoing·Stryker Howmedica Osteonics Corp.·August 1, 2012

ABG II Modular Hip Stem Stryker Howmedica Osteonics Corp. Mahwah, NJ 07430 Stryker Ireland Carrigtwohill Industrial Estate, Carrigtwohill County Cork, Ireland. The ABG II Modular range of implants is constituted of 8 right stems and 8 left stems. The necks are made of GADS Vitallium, a proprietary Co Cr alloy that Stryker has developed. GADS stands for Gas Atomized Dispersion Strengthened. IT is a Co Cr alloy that is a corrosion resistant and demonstrates qualities of improved fatigue strength (with respect to regular Co Cr alloy). Neck Range - The ABG II modular neck range is composed of 10 reversible neck implants. There are different options in terms of length, version and neck angle. The AG II Modular necks come in two different lengths: 28 mm (short) and 36 mm (long). The necks are offered in two version angles ; 0 and 7. The 0 and 7 necks are available in 125, 130 and 135 neck angles.

FDA Enforcement
Class II ·Ongoing·Stryker Howmedica Osteonics Corp.·August 1, 2012

TruDi NAV Suction, 0 Degrees; Model/Catalog Number: TDNS000Z. TruDi" NAV Suction Instruments are intended for use with the TruDi" Navigation System during surgical procedures in ENT medicine and skull base surgery

FDA Enforcement
Class II ·Ongoing·Integra LifeSciences Corp.·August 14, 2024

TruDi NAV Suction Instruments: 0-Degree, REF: TDNS000Z; 70-Degree, REF: TDNS070Z; and 90-Degree, REF: TDNS090Z

FDA Enforcement
Class II ·Ongoing·Acclarent, Inc.·December 29, 2021

Stryker Sustainability Solutions, BW Lasso 2515 NAV eco Variable Diagnostic EP Catheter, REF: D134301, ELECTRODES: 22, spacing:2-6-2MM, Length 115 cm, STERILE.EO, Rx Only

FDA Enforcement
Class II ·Ongoing·Stryker Sustainability Solutions·July 10, 2024

DR 800. Digital Radiography X-ray System.

FDA Enforcement
Class II ·Ongoing·Agfa N.V.·September 4, 2024

Barco MDSC-8527 NXF, Part Number K9352421

FDA Enforcement
Class II ·Ongoing·Barco N.V.·February 14, 2024

Agfa DX-D 100 system-Digital Radiography mobile X-ray System. A mobile X-Ray modality, consisting of X-Ray console, generator, tube, digital detector, and workstation. This modality is used to generate projection X-Ray images of human patients. Models: 5411/ 050, A5411/ 0300 and A5411/ 0400

FDA Enforcement
Class II ·Ongoing·Agfa N.V.·April 10, 2024

Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320, MNA-420 DEC -H V2/K9303331; MNA-440: MNA-440 ENC -H/K9303300, MNA-440 DEC -H V2/K9303311; MNA-620: MNA-620 DEC -H/K9306210, MNA-620 ENC -H/K9306220; and MNA-640: MNA-640 DEC -H/K9306410, MNA-640 ENC -H/K9306420; components of the NexxisOR system

FDA Enforcement
Class II ·Ongoing·Barco N.V.·July 2, 2025

V-Twin, REF 6002-800 or 6002-850, SN 18-3304, IVD, (01)03661540600180

FDA Enforcement
Class II ·Ongoing·Vital Scientific N.V.·December 4, 2019

V-Twin, Model # 6002-800, UDI: 03661540600180 Product Usage: An in-vitro diagnostic device, which is an automated chemistry analyzer, micro type, intended for clinical use in conjunction with certain materials to measure a variety of analytes, including applications in clinical chemistry, monitoring drugs of abuse and in therapeutic drug monitoring.

FDA Enforcement
Class II ·Ongoing·Vital Scientific N.V.·October 2, 2019

X-Guide Handpiece Adaptor Sleeve 3, Model P010727

FDA Enforcement
Class II ·Ongoing·X-NAV Technologies, LLC·April 10, 2024

X-Guide Handpiece Adaptor Sleeve 1, Model P010701

FDA Enforcement
Class II ·Ongoing·X-NAV Technologies, LLC·April 10, 2024

X-Guide X-Mark Probe Tool -used for registering edentulous patients to the software or performing XMark registration. Catalog Number:P010673

FDA Enforcement
Class II ·Ongoing·X-NAV Technologies, LLC·November 16, 2022

ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI code: 00190376476179; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use in surgical procedures. These instruments are non-sterile or sterile packaged, re-usable or single-use instruments designed to function with the Medtronic StealthStation System and NavLock Tracker.

FDA Enforcement
Class II ·Ongoing·Alphatec Spine, Inc.·February 18, 2026

ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 267-01-000-10-N UDI-DI code: 00190376541471; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use in surgical procedures. These instruments are non-sterile or sterile packaged, re-usable or single-use instruments designed to function with the Medtronic StealthStation System and NavLock Tracker.

FDA Enforcement
Class II ·Ongoing·Alphatec Spine, Inc.·February 18, 2026

Idylla INSTRUMENT, IVD, REF P0010. Intended for the detection of nucleic acid targets in various types of human samples, using disposable Test-specific ldylla Cartridges.

FDA Enforcement
Class II ·Ongoing·Biocartis Nv·January 22, 2025

Barco Medical Network Adapter, MNA-240, part of the NexxisOR system, Model Numbers: a) K9303078A, b) K9303097A

FDA Enforcement
Class II ·Ongoing·BARCO NV·October 5, 2022

Enterprise Imaging XERO Viewer- software application used for reference and diagnostic viewing of multispecialty medical imaging and non-imaging data . Enterprise Imaging XERO Viewer 8.0.0, 8.0.1, 8.1, 8.1.1, 8.1.2, 8.1.3,8.1.4, 8.2.0.000, 8.2.1.000, 8.2.2.000, 8.3.0.000, 8.3.1.000, 8.3.2.000, 8.4.0.000, 8.4.1.000 (including all SU s and HF s)

FDA Enforcement
Class II ·Ongoing·Agfa Healthcare NV·October 16, 2024

Agfa HealthCare Enterprise Imaging XERO Viewer

FDA Enforcement
Class II ·Ongoing·Agfa Healthcare NV·February 1, 2023