15 results
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18ms
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Sources: EU EUDAMED, US FDA
MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLE
FDA 510(k)
FDA Class 2
·Anesthesiology
Stern EX Acid Etched Implant RP 3.75x8.5mm, with cover screw, Ti
FDA UDI
STERNGOLD DENTAL LLC·00841549109041·The Sterngold Acid Etch Dental Implant System c...
Mini Master Series
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746106484·DB BKT MINI MS NARROW LOWER ANT 022 T=0 A=0 R=0
Rampart One Lumbar Interbody Fusion System
FDA UDI
SPINEOLOGY INC.·M7404901810·Variable Angle Drill
URISITE URINE COLLECTION KIT FOR MICROALBUMIN/CREATININE TESTING
FDA 510(k)
FDA Class 1
·Clinical Chemistry
3DHJD CAMERA SYSTEM MODEL
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523142514·Tesera X Trial, 60mm x 18mm x 10mm x 17°
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523141753·Tesera X Trial, 60mm x 18mm x 10mm x 0°
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523142019·Tesera X Trial, 60mm x 18mm x 10mm x 7°
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523142279·Tesera X Trial, 60mm x 18mm x 10mm x 12°
FLEXIMA? NASOBILIARY CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code FGE·June 30, 2014
TI PANGEA(TM) LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES BRANDYWINE·Product code NKB·January 8, 2013
LOW PROFILE SELF-TAPPING BONE SCREW
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·November 17, 2010
Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012
TRULIANT Knee System including TRULIANT Tibial Inserts, also labeled as the following: a. TRULIANT CR Tibial Inserts; b. TRULIANT CR Slope + Tibial Inserts; c. TRULIANT CR Slope ++ Tibial Inserts; d. TRULIANT CRC Tibial Inserts; e. TRULIANT PS Tibial Inserts; f. TRULIANT PSC Tibial Inserts. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·October 13, 2021