MAQ Surgical Instruments
Sialkot's 45-year surgical instrument maker, 6,000+ surgical, dental, and veterinary products.
MAQ Surgical Instruments is a veteran Sialkot manufacturer founded in 1978, producing over 6,000 surgical, dental, veterinary, and manicure instruments certified to ISO 9001:2000, cGMP, and CE standards. The company has grown into one of the fastest-growing surgical instrument exporters in Pakistan, supplying healthcare distributors, hospital procurement offices, and dental equipment wholesalers across the US, UK, Europe, and the Middle East. Sialkot's specialized workforce and tool-making tradition, dating back generations, underpins MAQ's competitive quality-to-price ratio.
- Type
- Manufacturer
- Location
- Sialkot, Pakistan
- Founded
- 1978
- Website
- maqsurgical.com
- Categories
- Medical & Healthcare Supplies, Tools & Equipment, Dental Supplies & Equipment
- Markets
- United States, United Kingdom, Germany, Australia, France, Italy, Netherlands, Sweden, Canada, United Arab Emirates
Verified facts
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-02 Domain registry record
- web-presence-since (green), checked 2026-08-09 Internet Archive (Wayback)
- registry-id-verified (green), checked 2026-08-19 FBR Active Taxpayer List (Federal Board of Revenue, Pakistan)
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- CE Marking EU NANDO (notified bodies)
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
- Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission