Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3043657402
- Devices
- 19
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd. makes
Neo Modulus produces the Augmented Gingival Matrix, a tissue-engineered scaffold designed for periodontal regeneration and soft tissue augmentation in dental procedures.
The company’s portfolio is regulated under FDA Class II devices, with the Augmented Gingival Matrix authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Search and filter all 19 devicesCompany details
- FDA FEI number
- 3043657402
- DUNS number
- 414744296
- Address
- Room 301, 302, Building 11, No. 8 Jinfeng Road, Suzhou City Jiangsu
Frequently asked questions
How many devices does Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd. have in the registry?
The registry currently lists 19 devices for Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd.'s devices?
Among its 19 most recently registered devices, Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (18 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd.'s devices fall under?
Among its 19 most recently registered devices, the classes recorded for Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd. in the registry?
The most recently registered devices listed for Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd. include Neocirrus AGM-R-020030, Neocirrus AGM-R-010040, Neocirrus AGM-R-010010 and Neocirrus AGM-R-010030.