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Data / Medical devices / Aligner, Bracket, Orthodontic / Pakistan

FDA-registered makers of Aligner, Bracket, Orthodontic in Pakistan: 12 establishments

12 establishments in Pakistan are registered with the FDA to make Aligner, Bracket, Orthodontic (product code ECQ). 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
Aligner, Bracket, Orthodontic
Product code
ECQ
Country
Pakistan

Makers of Aligner, Bracket, Orthodontic in Pakistan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Accompany SurgicalSIALKOT Punjab, PakistanManufacturer0000api.fda.gov
Acme EnterprisesSialkot Punjab, PakistanManufacturer0000api.fda.gov
Ameda Instruments CompanyKarachi Sindh, PakistanManufacturer0000api.fda.gov
Denta Craft InstrumentsSialkot Punjab, PakistanManufacturer0000api.fda.gov
Ghousia Amanat SurgicalSialkot Punjab, PakistanManufacturer0000api.fda.gov
Maryam TradingSIALKOT Punjab, PakistanManufacturer0000api.fda.gov
Medcave Private LimitedSialkot Punjab, PakistanManufacturer0000api.fda.gov
Melpex Beauty InstrumentsSialkot Punjab, PakistanManufacturer0000api.fda.gov
Panorama International.SIALKOT Punjab, PakistanManufacturer0000api.fda.gov
Richbolt EnterprisesSIALKOT Punjab, PakistanManufacturer0000api.fda.gov
SGS Export Intl.SIALKOT Punjab, PakistanManufacturer0000api.fda.gov
Zain's Medical ImageSIALKOT Punjab, PakistanManufacturer0000api.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.