PolyNovo
Biodegradable dermal matrices and wound care medical devices.
PolyNovo manufactures biodegradable dermal matrices and wound care medical devices from its Melbourne operations. The company supplies healthcare systems, laboratories, OEM partners or regulated export customers across its listed primary markets.
- Type
- Manufacturer
- Location
- Melbourne, Australia
- Founded
- 1998
- Website
- polynovo.com
- Categories
- Medical & Healthcare Supplies
- Markets
- Australia, United States, Germany, United Kingdom
Verified facts
- fda-registered (green), checked 2026-08-09 FDA
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- lei-lapsed (amber), checked 2026-08-23 GLEIF global LEI register (golden copy)
- domain-registered (green), checked 2026-08-09 Domain registry record
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- FDA Registered FDA Establishment Registration
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)