NovaPro 19512-32

by Nanova Biomaterials Inc

NovaPro 19512-32 is a Class II device made by Nanova Biomaterials Inc, listed in FDA GUDID since 30 Nov 2019 (UDI-DI 00816537021230), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00816537021230 UDI-DI	Date30 Nov 2019Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00816537021230

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: NovaPro
Generic name: Dental unfilled resin sealant/coating
Model / Ref / Catalog: 19512-32

Primary DI / UDI-DI: 00816537021230
FDA product code: EBC
GMDN term: Dental unfilled resin sealant/coating

Device class: Class II
Regulation number: 872.3765
GUDID distribution status: In Commercial Distribution

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Properties

Prescription use
Lot / batch number
Expiration date

Other properties (12, all answered No)