10,000 results · 16ms · Sources: EU EUDAMED, US FDA

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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