402 results · 8ms · Sources: EU EUDAMED, US FDA

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Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number: MHR 110-b Software Version: 1.5.0.0 Product Description: The Leaseir MHR Xcell is a surgical laser instrument for use in general and plastic surgery and dermatology, intended for hair removal and treatment of pseudo folliculitis barbae on all skin types (Fitzpatrick I-VI). The process implies the generation of intense light pulses at specific wavelengths. The specific nature of the energies and pulse durations cause the desired effect (in the hair follicles and oxyhemoglobin in the blood) heating them sufficiently and destroying them without unnecessary damage to surrounding tissue. This is achieved by controlled emission of laser radiation to the target tissue. The system consists of a main console and two interchangeable applicators that delivers pulsed light in the range of 800-820nm with a peak in the 810nm in different spot sizes. Two of the applicators emitting radiation at 810 nm wavelength for two areas 13.5¿15 mm¿ and 14.5¿25.5 mm¿. Two different operation modes are available: static mode and dynamic mode, which are differentiated basically by the frequency range defined for each mode (1-4 Hz for static and 10 Hz for dynamic). The principle of operation consists in the photons travel along the axis and reflected again back into the crystal, continuing the chain reaction, while photons travelling in different directions leave the crystal. In one of the two mirrors, a tiny hole allows a small amount of light to leak out and the resulting beam is focused with lenses and is emitted from the laser. The total energy emitted by the Leaseir MHR Xcell is produced by an array of diodes. The laser emission is activated by the hand piece trigger, deliver a continuous pulse pattern while the button is pressed. Component: NO

FDA Enforcement
Class II ·Completed·LEASEIR TECHNOLOGIES SLU·January 28, 2026

Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot 178713114 - 179433670

FDA Enforcement
Class II ·Completed·Beckman Coulter Mishima K.K.·June 11, 2025

Access Vitamin B12 Reagent, Catalog Number 33000, Lot Number 439850

FDA Enforcement
Class II ·Completed·Beckman Coulter, Inc.·July 23, 2025

AMT Initial Placement Dilator Set. Used to place gastrostomy devices.

FDA Enforcement
Class II ·Completed·Applied Medical Technology Inc·July 10, 2024

Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038

FDA Enforcement
Class II ·Completed·ESAOTE S.P.A.·March 11, 2026

Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201, 795231, 795232, 795234 REF: 795117, 795122

FDA Enforcement
Class II ·Completed·Philips Ultrasound, LLC·January 7, 2026

QC (80 kVp) screened nanoDot D2DNS, Model Number 03066-OTO; radiation monitoring dosimeter used with the microSTAR readers

FDA Enforcement
Class II ·Completed·Landauer·September 20, 2023

nanoDot D2DXN, Model Numbers: a) 03060-1MO; b) 03060-3MO; c) 03060-OTO; d) 03060-SMO; radiation monitoring dosimeter used with the microSTAR readers

FDA Enforcement
Class II ·Completed·Landauer·September 20, 2023

Calibrate (80 kVp) nanoDot D2DNS, Model Numbers: a) 18121-000; b)18121-KIT; c) 18121-SET; radiation monitoring dosimeter used with the microSTAR readers

FDA Enforcement
Class II ·Completed·Landauer·September 20, 2023

Stryker iBur 3.0mm Coarse Diamond Round, Distal Bend - intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and Endoscopic applications Ref: 8431-013-030DC

FDA Enforcement
Class II ·Completed·Stryker Corporation·September 4, 2024

Affiniti Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: Affiniti 30 795121 Affiniti 30 795218 Affiniti 50 795208 Affiniti 50 795118 Affiniti 70 795210 Affiniti 70 795119

FDA Enforcement
Class II ·Completed·Philips Ultrasound Inc·September 29, 2021

muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate

FDA Enforcement
Class II ·Completed·Murata Vios, Inc.·January 22, 2025

4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010

FDA Enforcement
Class II ·Completed·Acumed LLC·April 27, 2022

Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) Model # WC77, 2) Model # WC77D (Demo), 3) Model # WC77R (Refurbished); used in conjunction with Warming Blankets and Mattresses.

FDA Enforcement
Class II ·Completed·Augustine Temperature Management, LLC·January 22, 2025

Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) WC77V; 2) WC77V-DEMO; 3) WC77V-R; used in conjunction with Warming Blankets and Mattresses, veterinary use.

FDA Enforcement
Class II ·Completed·Augustine Temperature Management, LLC·January 22, 2025

Hillrom Temperature Management Controller, MP, Model # 2083516; used in conjunction with Warming Blankets and Mattresses.

FDA Enforcement
Class II ·Completed·Augustine Temperature Management, LLC·January 22, 2025

Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) Model # WC71, 2) Model # WC71R (refurbished); used in conjunction with Warming Blankets and Mattresses.

FDA Enforcement
Class II ·Completed·Augustine Temperature Management, LLC·January 22, 2025

Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) WC71V; 2) WC71V-DEMO; 3) WC71V-R; used in conjunction with Warming Blankets and Mattresses, veterinary use.

FDA Enforcement
Class II ·Completed·Augustine Temperature Management, LLC·January 22, 2025

INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup

FDA Enforcement
Class II ·Completed·Innomed, Inc.·May 8, 2024

Beckman Coulter DxI 9000 Access Immunoassay Analyzer, catalog number C11137; in-vitro diagnostic instrument

FDA Enforcement
Class II ·Completed·Beckman Coulter, Inc.·February 12, 2025