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Data / Medical devices / Punch, Biopsy, Surgical / India

FDA-registered makers of Punch, Biopsy, Surgical in India: 9 establishments

9 establishments in India are registered with the FDA to make Punch, Biopsy, Surgical (product code EME). 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
Punch, Biopsy, Surgical
Product code
EME
Country
India

Makers of Punch, Biopsy, Surgical in India

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Greens Surgicals Private LimitedVadodara Gujarat, IndiaManufacturer0000api.fda.gov
Gesco Healthcare Private LimitedCHENNAI, Tamil Nadu, IndiaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Hospital Equipment MFG. Co.NOIDA Uttar Pradesh, IndiaManufacturer0000api.fda.gov
Jai Surgicals Ltd.ALWAR Rajasthan, IndiaContract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler0000api.fda.gov
Meditec DevicesVasai(E), Thane, Maharashtra, IndiaContract manufacturer0000api.fda.gov
Razormed Inc.GURGAON Haryana, IndiaContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Ribbel International Ltd.SONEPAT Haryana, IndiaManufacturer0000api.fda.gov
Surgimed DevicesAHMEDABAD Gujarat, IndiaManufacturer0000api.fda.gov
Suru International Pvt LtdDAHANU Maharashtra, 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.