FDA Device Establishments · JSON-LD · Markdown

TEKIA, INC.

FEI 3002023310 · Manufacture Device in the United States for Export Only · Status: Active

FEI Number3002023310
Owner / OperatorTEKIA, INC (#10023535)
Address17 Hammond, suite 414, Irvine, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)HQL
Regulation § (21 CFR)886.3600
Proprietary namesTEKLENS III Hydrophobic Acrylic IOLs Model 900 series; TEKLENS II Three Piece Hydrophlic Acrylic IOLs Model 600 & 600Y Series; TEK-CLEAR Accommodative IOLs Model 500 Series; TEKLENS II Single Piece Hydrophlic Acrylic IOLs Model 800 & 800Y Series; TEKTOR Single Piece Acrylic Toric IOLs Model 820 &820Y

External sources

Source: openFDA. Public-domain (CC0).