91 results · 24ms · Sources: EU EUDAMED, US FDA

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Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·ANTERIOR CHAMBER INTRAOCULAR LENS (CATARACT)

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·ANTERIOR CHAMBER INTRAOCULAR LENS

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·ANTERIOR CHAMBER INTRAOCULAR LENS

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·ANTERIOR CHAMBER INTRAOCULAR LENS

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·ANTERIOR CHAMBER INTRAOCULAR LENS

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·ANTERIOR CHAMBER INTRAOCULAR LENS

Endo Carry-on Procedure Kit

FDA UDI
MEDIVATORS INC.·40677964054387·Endo Carry-on Procedure Kit Includes Basin, Enz...

NA

FDA UDI
Nuvasive, Inc.·00887517159847·NV IPAS III, Diamond Springless (Ster)

COMPRESSOR BOTTOM HANDLE

FDA UDI
Osteocentric Technologies, Inc.·00810097802421·COMPRESSOR BOTTOM HANDLE

infuset

FDA UDI
EMED TECHNOLOGIES CORPORATION·00817708021905·Infuset-3200 Flow Control Infusion set

Elite Expandable Interbody Fusion System

FDA UDI
SPINEOLOGY INC.·M7403010027·12mm Paddle Distractor

MAXIM KNEE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

UNKNOWN

FDA Adverse Event
Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·May 27, 2025

AUTOSOFT 90

FDA Adverse Event
Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·May 27, 2025

INSET II

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·October 17, 2025

INSET II

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·October 30, 2025

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·August 12, 2014

Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers

FDA Pre-Market Approval
FDA Class 2 ·ELECSYS FREE PSA IMMUNOASSAY/CALSET/CALCHECK

Kit, Test, Alpha-Fetoprotein For Neural Tube Defects

FDA Pre-Market Approval
FDA Class 3 ·IMMULITE/IMMULITE 1000 AFP AND IMMULITE 2000/IMMULITE 2500 AFP

SYRINGE 20ML LL 120/PKG

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 20, 2021