19 results · 44ms · Sources: EU EUDAMED, US FDA

Adtemp

FDA registration
AMERICAN DIAGNOSTIC CORP.·1 product·🇺🇸 United States

Probe Cover JZ-KBT-001,-002, -005, -007, -008, -009, -010, -015, -025, -026

FDA registration
SHENZHEN JUZHONG TECHNOLOGY CO.,LTD·1 product·🇨🇳 China

Probe Cover: JZ-KBT-001, JZ-KBT-002, JZ-KBT-005, JZ-KBT-007, JZ-KBT-008, JZ-KBT-009, JZ-KBT-010, JZ-KBT-015, JZ-KBT-025, JZ-KBT-026

FDA 510(k)
FDA Class 2 ·General Hospital

Persona Personalized Knee System TiNidium PS Femur

FDA registration
ZIMMER, INC.·2 products·🇺🇸 United States

clonoSEQ® Assay

FDA registration
ADAPTIVE BIOTECHNOLOGIES·1 product·🇺🇸 United States

clonoSEQ® Assay

FDA registration
ADAPTIVE BIOTECHNOLOGIES·1 product·🇺🇸 United States

Persona Femur CR Cemented Tivanium Standard

FDA registration
Sterigenics US, LLC·2 products·🇺🇸 United States

OSE

FDA UDI
ORTHODONTIC SUPPLY & EQUIPMENT COMPANY INC·00810042124769·EXPANDO RETRACTOR - LARGE #3

EVOS Lumbar Interbody System

FDA UDI
Cutting Edge Spine, LLC·00841193113418·HA PEEK EVOS Straight, ,9mmx8mmx 30mm , FLAT 0...

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112526·BARRON VACUUM TREPHINE 8.25MM

NA

FDA UDI
Stryker Trauma SA·07613154639724·Screw Marker 20,9

LensHooke Semen Test Cassette CS0;LensHooke Semen Test Cassette CS1

FDA registration
BONRAYBIO USA CORPORATION·1 product·🇺🇸 United States

A-CIFT® SoloFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361023692·A-CIFT SOLOFUSE IBFD, Lordotic 13mm Long, 17mm ...

3I IMPLANTS; OSSEOTITE DENTAL IMPLANTS; OSSEOTITE NT DENTAL IMPLANTS

FDA 510(k)
FDA Class 2 ·Dental

HP M2376A DEVICE LINK SYSTEM, MODEL M2376A

FDA 510(k)
FDA Class 2 ·Cardiovascular

TOSCA 500 PCO2, SPO2 AND PULSE RATE MONITORING SYSTEM, MODEL 5202009

FDA 510(k)
FDA Class 2 ·Anesthesiology

Continuous Measurement Thermometer

FDA classification
FDA Class 2 ·Continuous Measurement Thermometer

Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

FDA classification
FDA Class 2 ·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

Implant, Endosseous, Root-Form

FDA classification
FDA Class 2 ·Implant, Endosseous, Root-Form