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NV®PRO3 ZLR3003L

by Den-Mat Holdings, LLC

NV®PRO3 ZLR3003L is a Class II device made by Den-Mat Holdings, LLC, listed in FDA GUDID since 5 Jan 2017 (UDI-DI D813ZLR3003L0), 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

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD813ZLR3003L0 UDI-DI Date5 Jan 2017ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
NV®PRO3
Generic name
Dental diode laser system
Model / Ref / Catalog
ZLR3003L
Primary DI / UDI-DI
D813ZLR3003L0
FDA product code
GEX
GMDN term
Dental diode laser system
Device class
Class II
Regulation number
878.4810
GUDID distribution status
In Commercial Distribution

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Category: Dental diode laser system

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Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)