314 results · 22ms · Sources: EU EUDAMED, US FDA

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1688 Camera Control Unit ; 1688 AIM 4K Camera Head, C-Mount ; 1688 AIM 4K Camera Head with Integrated Coupler ; AIM 4K Coupler, 20mm, C-Mount ; L11 LED Light Source with AIM

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

1688 AIM 4K CAMERA HEAD WITH INTEGRATED COUPLER - INTERNATIONAL KIT

FDA Adverse Event
Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·September 13, 2024

PROPELLER HEAD SCREW SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304269576·

PILLING

FDA UDI
TELEFLEX INCORPORATED·24026704513158·

AccuQuest

FDA UDI
Bernafon AG·05711584078167·AQ CO9 MNR T, 2.4G NFM DPB SABE/MAC DEMO ACCUQ

BOSS Instruments

FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515026827·Lloyd-Davis Pelvis Ret,45/60x 130,11 3/4", w/li...

Ophthalmic Retractor

FDA UDI
KATENA PRODUCTS, INC.·00841668100967·DESMARRES LID RETRACTOR #1

n/a

FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM46001822061601·Rotary instrument for endodontic application

ZEUS-L

FDA UDI
SPINAL ELEMENTS·00840916134402·ZEUS®-L, Lateral Lumber Interbody Fusion Device...

ZEUS-L

FDA UDI
SPINAL ELEMENTS·00840916120672·ZEUS®-L Hyper, 18 x 21 x 60mm, 14 Degree

ZEUS-L

FDA UDI
SPINAL ELEMENTS·00840916134372·Zeus-L, Lateral Lumber Interbody Fusion Device,...

ZEUS-L

FDA UDI
SPINAL ELEMENTS·00840916141189·ZEUS® LLIF 18mm x 21mm x 60mm x 14° TRIAL

ZEUS-L

FDA UDI
SPINAL ELEMENTS·00840916141233·ZEUS® LLIF 18mm x 21mm x 60mm x 28° TRIAL

ZEUS-L

FDA UDI
SPINAL ELEMENTS·00840916141141·ZEUS® LLIF 18mm x 21mm x 60mm x 07° TRIAL

ZEUS-L

FDA UDI
SPINAL ELEMENTS·00840916141219·ZEUS® LLIF 18mm x 21mm x 60mm x 21° TRIAL

STRETCH VINYL EXAMINATION GLOVE POWDER FREE

FDA 510(k)
FDA Class 1 ·General Hospital

TAPERED SCREW-VENT X IMPLANT

FDA 510(k)
FDA Class 2 ·Dental

IMP TM 4.7MM MTX FULL, 11.5MM

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·November 25, 2022

IMP TM 4.7MM MTX FULL, 10

FDA Adverse Event
Injury ·ZIMVIE US CORP LLC·Product code DZE·April 23, 2026

IMP TM 4.7MM MTX FULL, 10

FDA Adverse Event
Injury ·ZIMVIE US CORP LLC·Product code DZE·April 23, 2026