10,000 results
·
16ms
·
Sources: EU EUDAMED, US FDA
LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SZ KKS SILICONE&ELECTRONIC CO., LTD.
FDA registration
SZ KKS SILICONE&ELECTRONIC CO., LTD.·2 products·🇨🇳 China
ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HSB·December 18, 2014
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·May 10, 2023
BD MAXZERO MULTI-FUSE EXTENSION SET WITH NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·September 27, 2024
BD MAXZERO MULTI-FUSE EXTENSION SET WITH NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·October 30, 2024
Histochemical PAS (Periodic Acid Schiff) Reaction Set. in vitro diagnostic. Product size configuration: Set of 4 bottles including Schiff Reagent 225mL, Light Green SF Yellowish Stain 225mL, Sodium Carbonate Solution 225mL, and Periodic Acid Solution 225mL. Each kit provides reagents sufficient for a maximum of 100 tests.
FDA Recall
Terminated
·EMD Chemicals Inc·Product code KKS·July 25, 2006
Acid, Periodic
FDA classification
FDA Class 1
·Acid, Periodic
SKS-Rehab AG
Manufacturer
🇨🇭 Switzerland
NG-International & Co. k.s.
Manufacturer
🇸🇰 Slovakia·1 Basic UDI-DI·1 Device
KLS Martin GmbH + Co. KG
Manufacturer
🇩🇪 Germany·1 Basic UDI-DI·1 Device·DQS Medizinprodukte GmbH
Beijing KES Biology Technology Co.,Ltd.
Manufacturer
🇨🇳 China·6 Basic UDI-DIs·6 Devices·TÜV SÜD Product Service GmbH, TÜV SÜD Product Service GmbH, and TÜV SÜD Product Service GmbH
BKS FABRICS PRIVATE LIMITED
FDA registration
BKS FABRICS PRIVATE LIMITED·1 product·🇮🇳 India
BEIJING KES BIOLOGY TECHNOLOGY CO., LTD.
FDA registration
BEIJING KES BIOLOGY TECHNOLOGY CO., LTD.·2 products·🇨🇳 China
GM-K2 S
Device
EU MDR
·
Eu Md Class 1
·PATELLA-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság·On the market
GM-K8 S
Device
EU MDR
·
Eu Md Class 1
·PATELLA-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság·On the market
BKS Revision System
FDA 510(k)
FDA Class 2
·Orthopedic
SO telesc. smoke evac. handle, NSTC,4.5m
Device
EU MDD
·
Eu Md Class 2b
·KLS Martin GmbH + Co. KG·On the market·32 countries
Back Tape
Device
EU MDR
·
Eu Md Class 1
·NG-International & Co. k.s.·On the market
CONTINUUM KNEE SYSTEM (CKS)
FDA 510(k)
FDA Class 2
·Orthopedic