ClearanceBrief
Company · US

International Medical Industries, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2017 to 2024. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)

Product codes

CodeDeviceRecords
FMFSyringe, Piston2
LHISet, I.V. Fluid Transfer2
FPASet, Administration, Intravascular1
KPEContainer, I.V.1
PNREnteral Syringes With Enteral Specific Connectors1
QEHPiston Syringe With Neuraxial Connector – Epidural, Peripheral, And/Or Indirect Cerebral Spinal Fluid Contact1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 4, 2024K231095Tamper Evident Cap
International Medical Industries, Inc.
FMF
Dec 16, 2020K201031NRFit® Caps, Male and Female Neuraxial Tip Caps
International Medical Industries, Inc.
QEH
Jan 31, 2020K193192Tamper Evident Cap
International Medical Industries, Inc.
FMF
Apr 30, 2019K190305Additive Cap
International Medical Industries, Inc.
KPE
Jan 11, 2019K182545Tamper Evident Cap with Male Luer Lock
International Medical Industries, Inc.
FPA
Jun 7, 2018K173577Guarded Luer Connector
International Medical Industries, Inc.
LHI
Oct 6, 2017K170672Tamper Evident Cap For use with ENFit Syringes
International Medical Industries, Inc.
PNR

Latest recalls

DateFirm and productCodeLinked 510(k)
Jan 7, 2023International Medical Industries, Inc.
Prep-Fill Guarded Luer Connector (GLC): a. Part Number 57-400, Female Lock - Female Lock Guarded Luer Connector, Sterile; b. Part number 57-400W, Female Lock - Female Lock Guarded Luer Connector,
Open, Classified
LHIK173577
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