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Contamac, Ltd.

Country not established FDA

Devices
20
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

Catalogue20

Newest first, rows 1-20 of 20

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Rows 1-20 of 20

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Contamac Ltd. ESSEX UK · GB FEI 3001190611

Frequently asked questions

How many devices does Contamac, Ltd. have in the registry?

The registry currently lists 20 devices for Contamac, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Contamac, Ltd.'s devices?

Among its 20 most recently registered devices, Contamac, Ltd. has devices listed in FDA 510(k) (18 devices) and FDA PMA (2 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Contamac, Ltd.'s devices fall under?

Among its 20 most recently registered devices, the classes recorded for Contamac, Ltd.'s devices are Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Contamac, Ltd. in the registry?

The most recently registered devices listed for Contamac, Ltd. include CONTAFLEX 55 (METHAFILCON) SPHERICAL SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND TINTED, LATHE-CUT), OPTIMUM GP (roflufocon D, roflurocon E) Daily Wear Contact Lens, HEXA100 (hexafocon A) Daily Wear Contact Lens, CONTAFLEX 38 (POLYMACON) SPHERICAL SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND TINTED, LATHE-CUT) and CONTAFLEX 54 (hioxifilcon D) Spherical Soft Contact Lens for Daily Wear, CONTAFLEX 49 (hioxifilcon B) Spherical Soft Contact Lens for Daily Wear,.

Which FDA establishments are linked to Contamac, Ltd.?

1 FDA establishment is linked to Contamac, Ltd. in the registry; they are listed on the company page.

Generated automatically from registry data and not verified by a human reviewer.