55 results · 25ms · 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.

Tekia, Inc.

Manufacturer
🇺🇸 United States·16 Basic UDI-DIs·16 Devices·3 Importers·GMED SAS, GMED SAS, GMED SAS, and GMED SAS

TEKIA, INC.

FDA registration
TEKIA, INC.·1 product·🇺🇸 United States

Tek-Lens II

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·12 countries

Tek-Lens III

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·6 countries

Tek-Clear

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·8 countries

Ophthalmo Pro

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·2 countries

MeyeLens

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·2 countries

Tek-Lens II

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·6 countries

Tek-Lens II

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·11 countries

Tek-Lens II

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·11 countries

Tek-Lens II

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·11 countries

Tek-Lens II

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·11 countries

Tek-Lens II

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·4 countries

Tek-Lens II

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·9 countries

Tek-Lens II

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·9 countries

Tek-Lens II

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·8 countries

Tek-Lens II

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·9 countries

Tek-Lens II

Device
EU MDD · Eu Md Class 2b ·Tekia, Inc.·On the market·9 countries

TEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile. The firm name on the label is TEKIA, INC., Irvine, CA.

FDA Enforcement
Class II ·Terminated·Tekia, Inc.·December 25, 2019

TEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile. The firm name on the label is TEKIA, INC., Irvine, CA.

FDA Recall
Terminated ·Tekia, Inc.·Product code HQL·November 9, 2018