510(k) clearances

LithoVue Elite Digital Flexible Ureteroscope System

Boston Scientific Corporation · Gastroenterology, Urology

K261153Substantially EquivalentTraditionalFGB
Open FDA's page for this record
Third party flag
N
City
Marlborough
Advisory committee description
Gastroenterology, Urology
Address 1
300 Boston Scientific Way
Statement or summary
Summary
Product code
FGB
Zip code
01752
Applicant
Boston Scientific Corporation
Decision date
2026-08-26
Decision code
SESE
Country code
US
Device name
LithoVue Elite Digital Flexible Ureteroscope System
Advisory committee
GU
Contact
Avinash Purohit
K number
K261153
State
MA
Date received
2026-04-08
Review advisory committee
GU
Postal code
01752
Decision description
Substantially Equivalent
Clearance type
Traditional
Harmonized identifiers (openFDA)
Device name
Ureteroscope And Accessories, Flexible/Rigid
Medical specialty description
Gastroenterology, Urology
Regulation number
876.1500
Device class
2
Registration number
3017425975, 8043903, 3014683069, 3013992977, 3013247477, 3017210488, 3005580113, 3011986317, 3032959393, 3014893827, 3010220595, 1000121056, 3012797688, 9616693, 3021246306, 3004040397, 3004111573, 3014644276, 1418479, 1820334, 3010421104, 3021031769, 3025349506, 3032429484, 3022106566, 3012322232, 3020746799, 3037966040, 2936485, 3004361445, 2531475, 3017367014, 3012843412, 3015139943, 3003206812, 9610773, 3008776287, 3042940358, 3002808148, 9610595 +81 more
FEI number
3014683069, 3013992977, 3002808273, 3013247477, 3017210488, 3005580113, 3003922255, 3011986317, 3032959393, 3014893827, 3010220595, 1000121056, 3012797688, 3021246306, 3008185830, 3004040397, 3004111573, 1418479, 1820334, 3010421104, 3021031769, 3025349506, 3032429484, 3022106566, 3012322232, 3020746799, 3037966040, 2936485, 3004361445, 3017367014, 3006149253, 3015139943, 3012843412, 3003206812, 3006759904, 3008776287, 3002808268, 3007475226, 3002806565, 3002808148 +81 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.