ClearanceBrief
Company ยท US

Isoaid, LLC

FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2025. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KXKSource, Brachytherapy, Radionuclide6

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 15, 2025K242818IsoSphere
Isoaid, LLC
KXK
Dec 5, 2014K141701I-125 RSLN [RADIOACTIVE SEED AND LOCALIZATION NEEDLE]
Isoaid, LLC
KXK
Aug 10, 2012K113210ADVANTAGE-STRAND/ADVANTAGE-LOAD BRACHYTHERAPY KIT
Isoaid, LLC
KXK
Sep 15, 2009K091117ADVANTAGE-STRAND/ ADVANTAGE-LOAD BRACHYTHERAPY KIT, MODEL IASLBKA
Isoaid, LLC
KXK
Apr 8, 2004K033770ISOAID ADVANTAGE PD-103, MODEL IAPD-103A
Isoaid, LLC
KXK
Jul 10, 2001K011205ISOAID IODINE BRACHTHERAPY SEEDS, MODEL ADVANTAGE I-125
Isoaid
KXK

Latest recalls

DateFirm and productCodeLinked 510(k)
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