NeuLight® 099071

GUDID 02816901024056

Weinert Fiber Optics, Inc.

Urogenital surgical laser system beam guide, reusable
Primary Device ID02816901024056
NIH Device Record Keyae2ef375-5de6-45f6-9f57-5d4a24bff40d
Commercial Distribution StatusIn Commercial Distribution
Brand NameNeuLight®
Version Model NumberWFR-200-SB
Catalog Number099071
Company DUNS039281260
Company NameWeinert Fiber Optics, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100816901024058 [Primary]
GS101816901024057 [Package]
Contains: 00816901024058
Package: [5 Units]
In Commercial Distribution
GS102816901024056 [Package]
Contains: 01816901024057
Package: [2 Units]
In Commercial Distribution

FDA Product Code

GEXPowered laser surgical instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-12-30
Device Publish Date2024-12-22

On-Brand Devices [NeuLight®]

01816901023371WFS-365-RTSB
01816901023906WFS-365-SB
02816901023882WFR-365-SB
01816901023876WFR-200-SB
02816901023868WFS-272-RTSB
02816901023851WFR-272-SB
02816901023387WFS-272-RTSB
02816901023950WFS-200-SB
02816901023943WFR-600-SB
02816901023936WFS-200-RTSB
02816901023714WFS-600-SF
01816901023845WFS-940-RTSB
01816901023722WFS-550-SB
01816901023395WFS-940-SB
02816901023967WFS-550-RTSB
01816901023975WF IR600/630ST-3/SM-F 1030X3S
02816901024056WFR-200-SB
02816901024049WFS-200-SB

Trademark Results [NeuLight]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NEULIGHT
NEULIGHT
98519901 not registered Live/Pending
Neulight, LLC
2024-04-25
NEULIGHT
NEULIGHT
87679826 not registered Dead/Abandoned
Neulight, LLC
2017-11-10
NEULIGHT
NEULIGHT
79371304 not registered Live/Pending
Weinert Industries AG
2023-01-18
NEULIGHT
NEULIGHT
79370342 not registered Live/Pending
Weinert Industries AG
2022-11-11

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.