ClearanceBrief
Company ยท US

Alembic, LLC

FDA 510(k) clearances and medical device recalls filed under this name, 2023 to 2026. Name variants (Inc, Corp, punctuation) are merged.

13510(k) clearances (3 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
NRYCatheter, Thrombus Retriever7
DQYCatheter, Percutaneous4
QJPCatheter, Percutaneous, Neurovasculature2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 6, 2026K261938APRO 88 Catheter
Alembic, LLC
QJP
Aug 12, 2026K262392APRO 35 Swift Catheter
Alembic, LLC
DQY
Aug 12, 2026K262391APRO 35 Swift Catheter and Alembic Aspiration Tubing
Alembic, LLC
NRY
May 1, 2025K251014APRO 45 Catheter
Alembic, LLC
DQY
Apr 30, 2025K251015APRO 45 Catheter and Alembic Aspiration Tubing
Alembic, LLC
NRY
Apr 29, 2025K250962APRO 55 Intermediate Catheter
Alembic, LLC
DQY
Apr 28, 2025K250958APRO 55 Swift Catheter and Alembic Aspiration Tubing
Alembic, LLC
NRY
Feb 24, 2025K243287APRO 70 Swift Catheter and Alembic Aspiration Tubing
Alembic, LLC
NRY
Jan 14, 2025K243297APRO 70 Swift Catheter
Alembic, LLC
QJP
Mar 15, 2024K234115APRO 55 Catheter
Alembic, LLC
DQY
Feb 29, 2024K232971APRO 55 Catheter and Alembic Aspiration Tubing
Alembic, LLC
NRY
Apr 10, 2023K230695APRO 70 Catheter and Alembic Aspiration Tubing
Alembic, LLC
NRY
Feb 17, 2023K223545APRO 70 Catheter and Alembic Aspiration Tubing
Alembic, LLC
NRY

Latest recalls

DateFirm and productCodeLinked 510(k)
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