33 results · 26ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

MEDICAL PLATES, LATERAL PLATES, POSTERIOR LATERAL PLATES, OLECRANON PLATES MODEL 131218704-708; 851318704-708, 131218204

FDA 510(k)
FDA Class 2 ·Orthopedic

HHM

FDA UDI
Oticon A/S·05707131164315·K130, RITE CNB HHM

JOBST Bella Lite

FDA UDI
BSN MEDICAL, INC.·00035664002343·BELLA LITE 20-30 MM HG ARMSLEEVE WITH BAND LARG...

Clearflo PFT Filter in bag

FDA UDI
Thorasys Thoracic Medical Systems Inc·07540261014215·Clearflo PFT Filter. Used with tremoFlo Airwav...

Stainless Steel Archwires

FDA UDI
Ortho Organizers, Inc.·00190707065614·.019 X .025 Lower Bright Stainless Steel Oval A...

Symmetry Olsen

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00841785101250·

Orthoquest

FDA UDI
Young Innovations, Inc.·00843471156148·V D-Form 018X018

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450457870·

GUTTA PERCHA POINTS

FDA UDI
DiaDent Group International·08806383500975·Gutta Percha Points is used to root canal filin...

Stryker

FDA UDI
Provision·B504OM22961014210·

Young Specialties

FDA UDI
Young Innovations, Inc.·00840326425893·NiTi SE Archwire, D-FORM .018x.018 10EA

NA

FDA UDI
STERILMED, INC.·10888551037044·BUR CARBIDE CROSS CUT FISSURE LONG 6 FLUTES

POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

FDA 510(k)
FDA Class 1 ·General Hospital

ONTRAK TESTCUP 501, MODEL 3016633

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

E SERIES DEFIBRILLATOR

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION, WORLD WIDE HEADQUARTERS·Product code MKJ·April 29, 2013

GRANUFLO

FDA Adverse Event
Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 3, 2014

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·May 24, 2011

PERCEPT

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·July 9, 2021

ACTIVA

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·July 1, 2021

TURBO-JECT® DOUBLE LUMEN BEDSIDE POWER-INJECTABLE PICC

FDA Adverse Event
Injury ·COOK INC·Product code LJS·November 29, 2018