23 results · 28ms · Sources: EU EUDAMED, US FDA

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MODEL FAMILY OF AEROLASE ND:YAG LASERS: FRIENDLYLIGHT ND: YAG LASERS, FRIENDLYLIGHT NEO, LIGHTPOD ND: YAG LASERS, LIGHTP

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772777525·LUMBAMED PLUS FLEX PAD M SILVER V

JOBST soSoft

FDA UDI
BSN MEDICAL, INC.·00035664007904·SOSOFT 20-30 MM HG KNEE HIGH RIB LARGE SAND 1 E...

ARGENCO 52 (5 dwt)

FDA UDI
ARGEN CORPORATION, THE·D818120235·Gold based noble metal

N/A

FDA UDI
Tyber Medical, LLC·M695M1202350·

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197033213·Enterotomy scissors 21.0 c...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197540063·Cushing Laminectomy Ronguer 5x10mm 230mm

FILTEK SUPREME ULTRA FLOWABLE RESTORATIVE

FDA 510(k)
FDA Class 2 ·Dental

A1CNOW FOR PROFESSIONAL USE

FDA 510(k)
FDA Class 2 ·Hematology

Truliant

FDA UDI
Exactech, Inc.·10885862314796·Truliant PS Porous Femoral

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·December 19, 2023

TRULIANT PS POR FEM PS POR LEFT SZ 3.5

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code MBH·September 14, 2022

PROXIMATE ILS CURVED CIR STAPL

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 20, 2013

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·September 26, 2014

PRG INLIN ASD PLATFORM VO

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF, INC., MEDOS S.A.·Product code JXG·June 7, 2011

TRULIANT POR TIB TRAY SIZE 3.5F/3.5T

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·January 2, 2025

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·July 2, 2025

TRULIANT PS POR FEM PS POR LEFT SZ 3.5

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·January 6, 2025

ECHELON ENDOPATH

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 1, 2017

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·July 2, 2025