FDA Device Establishments · JSON-LD · Markdown

ELTECH K-LASER S.R.L.

FEI 3004642415 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active

FEI Number3004642415
Owner / OperatorELTECH K-LASER, S.R.L. (#9067781)
AddressVIA CASTAGNOLE, 20/H-INTERNO 2, TREVISO, 31100, IT
Mandatory US AgentK-LASER USA INC
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)ILY, GEX
Regulation § (21 CFR)890.5500, 878.4810

External sources

Source: openFDA. Public-domain (CC0).