Every instrument sold by Nexodent is manufactured to surgical-grade standard and supplied through channels compliant with the Therapeutic Goods Administration (TGA) and the Australian Register of Therapeutic Goods (ARTG).

Nexodent Gracey Curette, TGA listed surgical instrument

What TGA Listing Means

The TGA regulates therapeutic goods supplied in Australia, including reusable surgical and dental instruments classified as medical devices. TGA listing confirms a product has met the applicable regulatory requirements for supply in the Australian market.

What ARTG Registration Means

The ARTG is the public register of therapeutic goods approved for supply in Australia. A product's ARTG entry is the reference point clinics and procurement teams can check to confirm a device is legally supplied.

ARTG entry number(s): [FILL IN: your ARTG number(s), or a statement such as "available on request — contact us for the certificate"].

Material & Manufacturing Standard

  • Surgical-grade stainless steel construction
  • Individually inspected instruments
  • Autoclavable — see our sterilization & care guide
  • [FILL IN: specific steel grade if you publish one, e.g. German or Pakistani stainless, and any ISO/manufacturing certification you hold]

Why This Matters When Ordering

For clinics and procurement teams, regulatory listing is part of due diligence before an instrument enters clinical use. Confirming TGA/ARTG status up front avoids delays at the ordering or compliance-review stage.

Verify or Request Documentation

If you need a copy of our TGA listing or ARTG certificate for your practice's procurement records, contact us and we'll send it directly. [FILL IN: support email or link to your contact page]