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Icm Pharma Pte, Ltd.

SingaporeFDA 510(k) applicant, unverified FDA

Devices
4
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Icm Pharma Pte, Ltd. makes

Icm Pharma Pte, Ltd. manufactures SuperSlyde Personal Lubricant, a topical lubricating gel designed for medical and personal use to reduce friction and discomfort during procedures or intimate activities.

The company’s product portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. The manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

Company details

DUNS number
595170135

FDA establishments1

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

  • Icm Pharma Pte Ltd Singapore Central Singapore · SG FEI 3011318803

Frequently asked questions

How many devices does Icm Pharma Pte, Ltd. have in the registry?

The registry currently lists 4 devices for Icm Pharma Pte, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Icm Pharma Pte, Ltd.'s devices?

Among its 4 most recently registered devices, Icm Pharma Pte, Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Icm Pharma Pte, Ltd.'s devices fall under?

Among its 4 most recently registered devices, the classes recorded for Icm Pharma Pte, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Icm Pharma Pte, Ltd. in the registry?

The most recently registered devices listed for Icm Pharma Pte, Ltd. include SuperSlyde Personal Lubricant.

Which FDA establishments are linked to Icm Pharma Pte, Ltd.?

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

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