Alembic, LLC

FDA Regulatory Profile

Alembic, LLC appears in FDA public data with 0 recalls, 12 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Aug 12, 2026.

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Known Names

Alembic, Alembic Pharmaceuticals Limited, Alembic Therapeutics

Recent 510(k) Clearances

K-NumberDeviceDate
K262391APRO 35 Swift Catheter and Alembic Aspiration TubingAug 12, 2026
K262392APRO 35 Swift CatheterAug 12, 2026
K251014APRO 45 CatheterMay 1, 2025
K251015APRO 45 Catheter and Alembic Aspiration TubingApr 30, 2025
K250962APRO 55 Intermediate CatheterApr 29, 2025
K250958APRO 55 Swift Catheter and Alembic Aspiration TubingApr 28, 2025
K243287APRO 70 Swift Catheter and Alembic Aspiration TubingFeb 24, 2025
K243297APRO 70 Swift CatheterJan 14, 2025
K234115APRO 55 CatheterMar 15, 2024
K232971APRO 55 Catheter and Alembic Aspiration TubingFeb 29, 2024
K230695APRO 70 Catheter and Alembic Aspiration TubingApr 10, 2023
K223545APRO 70 Catheter and Alembic Aspiration TubingFeb 17, 2023