10,000 results · 81ms · 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.

CT-190G CELLULOSE TRIACETATE

FDA Adverse Event
Injury ·NIPRO CORPORATION USD·Product code MSF·January 25, 2008

Medline Convenience kits labeled as: 1) OR CLEAN UP KIT, Pack Number DYK1002355X3, 2) CLEANING & CUTTING, Pack Number DYNJ84657

FDA Recall
Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code OKG·April 8, 2024

Medline medical procedure kits labeled as follows: a) TURNOVER KIT, REF DYKC1289F

FDA Recall
Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code OKG·March 22, 2024

Medline convenience kits containing semi-rigid suction liners labeled as follows: ANES TURNOVER KIT-LF, Pack Number DYNJAA10338J

FDA Recall
Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code OKG·June 27, 2024

Body Fluid Clean Up Kit

FDA classification
FDA Class 2 ·Body Fluid Clean Up Kit

Prosthetic Silicone Materials

FDA UDI
TECHNOVENT LIMITED·05060483012162·Silicone materials for manufacture of adhesive ...

Denture Base Polymers

FDA UDI
SHANDONG HUGE DENTAL MATERIAL CORPORATION·06970402678036·

Prosthetic Silicone Materials

FDA UDI
TECHNOVENT LIMITED·05060483012094·Silicone materials for manufacture of adhesive ...

Denture Base Polymers

FDA UDI
SHANDONG HUGE DENTAL MATERIAL CORPORATION·06970402677817·

Prosthetic Silicone Materials

FDA UDI
TECHNOVENT LIMITED·05060483012117·Silicone materials for manufacture of adhesive ...

WAKAKUSA MOXA

FDA UDI
YAMASHO CO.,LTD.·04979844116085·

dima Print Splint clear

FDA UDI
pro3dure medical GmbH·EPRC66077916·Light curing liquid for 3D-printing

PRO3DURE GR-21 Try-In

FDA UDI
pro3dure medical GmbH·EPRCD1001601·printodent GR-21 Try-In 1kg ; color:A2

PRO3DURE GR-22 flex

FDA UDI
pro3dure medical GmbH·EPRCD1001701·printodent GR-22 flex

Elastomeric Impression Material

FDA UDI
SHANDONG HUGE DENTAL MATERIAL CORPORATION·06970402670047·

CKG CARDIOKYMOGRAPH

FDA 510(k)
FDA Class 2 ·Cardiovascular

APPLICARD (EKG)

FDA 510(k)
FDA Class 2 ·Cardiovascular

EKG SPEAKS

FDA 510(k)
FDA Class 2 ·Cardiovascular

CKG 8800

FDA 510(k)
FDA Class 2 ·Cardiovascular

CKG 8000

FDA 510(k)
FDA Class 2 ·Cardiovascular