Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
2026830689
Device Listing 2026830689
Listing Summary
#
Listing key
2026830689
Premarket submission
K241244
Device
CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter
Applicant
Cerenovus, Inc.
Product code
QJP
Decision date
2024-10-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
168757
3007628272
3007628272
Cerenovus, Inc.
1
N
2026-01-01
6303 Waterford District Drive Suites 215 and 315 Miami FL US 33126
114891
3008264254
3008264254
Cerenovus, Inc.
1
N
2026-01-01
Calle Circuito Interior Norte #1820 Parque Industrial Salvarcar Ciudad Juarez, Chihuahua Mexico MX C.P. 32574