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
1627860289
Device Listing 1627860289
Listing Summary
#
Listing key
1627860289
Premarket submission
K243893
Device
Second OpinionĀ® Pediatric
Applicant
Pearl, Inc.
Product code
MYN
Decision date
2025-05-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
303491
3021887566
3021887566
PEARL INC.
1
N
2026-01-01
9200 W Sunset Blvd Ste 430 West Hollywood CA US 90069