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Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Female (CH06 - CH16); Cure Aqua™ Ready to Use Hydrophilic Inte

Convatec

Summary

Convatec received 510(k) clearance for Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Female (CH06 - CH16); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Straight (CH06 - CH18); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Coude (CH10 - CH18)., a EZD device. Cleared on 2026-08-05.

Details

Source

510(k) Clearance

External ID

K260737

Action Date

2026-08-05

Status

Traditional

Category

device

Product Code

EZD

Product Description

Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Female (CH06 - CH16); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Straight (CH06 - CH18); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Coude (CH10 - CH18).. Product code: EZD.

Company

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 400 device clearances issued this month. Convatec has received 4 total clearances in our database.

Convatec has 4 FDA actions in our database, including 4 clearances.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Convatec have FDA actions?

Convatec has 4 FDA actions in our database, including 0 recalls and 4 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K260737" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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