Skip to the page

Data / Medical devices / Garment, Protective, For Incontinence / India

FDA-registered makers of Garment, Protective, For Incontinence in India: 11 establishments

11 establishments in India are registered with the FDA to make Garment, Protective, For Incontinence (product code EYQ). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Garment, Protective, For Incontinence
Product code
EYQ
Country
India

Makers of Garment, Protective, For Incontinence in India

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Dynamic Techno Medicals Private LimitedCoimbatore Tamil Nadu, IndiaContract manufacturer, Manufacturer0000api.fda.gov
Dynamic Techno Medicals Pvt. LtdErode Tamil Nadu, IndiaContract manufacturer, Manufacturer0000api.fda.gov
Lords Mark Industries Ltd.Daman and Diu Dadra and Nagar Haveli, IndiaManufacturer0000api.fda.gov
M/S. Ascent Meditech LimitedGOREGAON (E) Maharashtra, IndiaManufacturer0000api.fda.gov
Narang Medical, Ltd.New Delhi, IndiaManufacturer0000api.fda.gov
Pan Healthcare Private LimitedBiliyada Gujarat, IndiaContract manufacturer, Manufacturer0000api.fda.gov
Sekhani Industries Pvt LtdAhmedabad Gujarat, IndiaManufacturer0000api.fda.gov
SPM Medicare Pvt, Ltd.NOIDA Uttar Pradesh, IndiaManufacturer0000api.fda.gov
Solis Hygiene Pvt. Ltd.Dhar Indore Madhya Pradesh, IndiaContract manufacturer0000api.fda.gov
Swara Baby Products LimitedDhar Indore Madhya Pradesh, IndiaContract manufacturer0000api.fda.gov
WW Group UkTirupur Tamil Nadu, IndiaManufacturer0000api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.