Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016445722

FEI Number

3016445722

Entity Name

OSMUNDS

City/State/Country

Riga, LV

Establishment Address

Siltuma iela 4, Riga LV 1058, LV

Establishment Type(s)

Sterilize Medical Device for Another Party (Contract Sterilizer)

Owner / Operator

Osmunds (Owner Number: 10056745)

Owner / Operator Contact Address

Siltuma iela 4, Riga, LV-RIX LV 1058, LV

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Auryon Atherectomy Catheter with/without aspiration 2.35 mm OTW B-Laser catheter 0.9 mm OTW B-Laser catheter 1.5 mm OTW B-Laser catheter 2 mm OTW B-Laser catheter Auryon Atherectomy Catheter 1.5mm, XL (Extra long) - Hydrophilic coated Auryon Atherectomy Catheter 2.35mm OTW Auryon Atherectomy Catheter 2.35mm - Hydrophilic coated Auryon Atherectomy Catheter 2mm OTW Auryon Atherectomy Catheter 0.9mm OTW Auryon Atherectomy Catheter 2mm - Hydrophilic coated Auryon Atherectomy Catheter 0.9mm, XL (Extra long) - Hydrophilic coated Auryon Atherectomy Catheter 1.5mm, XL (Extra long) Auryon Atherectomy Catheter 1.5mm OTW Auryon Laser System - for Infra Inguinal Atherectomy Auryon Atherectomy Catheter 1.5mm - Hydrophilic coated Auryon Atherectomy Catheter 0.9mm - Hydrophilic coated

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MCW	Catheter, Peripheral, Atherectomy	Cardiovascular	Class 2	870.4875	2022-07-07
GEX	Powered Laser Surgical Instrument	General, Plastic Surgery	Class 2	878.4810	2020-01-03
MCW	Catheter, Peripheral, Atherectomy	Cardiovascular	Class 2	870.4875	2020-12-01
MCW	Catheter, Peripheral, Atherectomy	Cardiovascular	Class 2	870.4875	2024-01-02

Official Correspondent

No official correspondent registered.

US Agent Details

Darshan Bhaiya Business: MAE Group Email: darshanb@maegroups.com Phone: (603) 5050730

Related Public Records

Same Entity

Osmunds

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K083258	Dornier Medtech America, Inc.	MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE	2009-01-30
K201111	Candela Corporation	GentleMax Pro Plus	2020-05-26
K202758	Shangdong Huamei Technology Co., Ltd.	Nd: YAG Laser Therapy Systems HM-YL900	2020-11-16
K904068	Luxar Corp.	LUXAR MODEL LX-20 CO2 LASER	1991-04-15
K142225	CAO Group, Inc.	Pilot Elite Diode Laser	2014-09-12

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0005-2014	PhotoMedex, Inc.	2	The product is labeled in part "*Surgical Laser Technologies, Inc. Montgomeryville, PASLT Fiber Delivery SystemSterileNon-Pyrogenic**. The product is packaged in a flexible pouch and includes the following laser surgery accessories - SLT-SSRH 8, Catalog/Product Number 0041-3082; SLT-SSRH 11, Catalog/Product Number 0041-3112; SLT-SSRH 4-SMA, Catalog/Product Number 0042-0075; SLT-SSRH 5-SMA, Catalog/Product Number 0042-0076; SLT-SSRH 6-SMA, Catalog/Product Number 0042-0077; SLT-SSRH 7-SMA, Catalog/Product Number 0042-0078; SLT-SSRH 8-SMA, Catalog/Product Number 0042-0079; SLT-SSRH 9-SMA, Catalog/Product Number 0041-4931; and SLT-SSRH 10-SMA, Catalog/Product Number 0042-0081. Indicated for the incision, excision, coagulations, and vaporization of soft tissue.
Z-0025-2018	Medtronic Navigation, Inc.	2	VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559 Visualase Cooled Laser Applicator System 3mm Tip; Part Number: 9735560 Visualase Cooled Laser Applicator System 10mm Tip; Part Number: 9735561 Visualase Cooled Laser Applicator System 15mm Tip
Z-0028-2007	Lumenis Inc.	2	Lumenis brand DuoTome SideLite 550 Micron Delivery System; laser systems for ablating soft tissue. Catalog Number: 0641-800-01; Manufactured by Lumenis, Inc., 2400 Condensa Street, Santa Clara, CA

Similar Registrations

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3004091615	Abbott Vascular Netherlands	Heerlen Limburg, NL
3002807314	Synergy Health Ireland Ltd	Tullamore Offaly, IE
2011171	Sterigenics US LLC	Los Angeles, CA, US
3012669557	LIGHT GUIDE OPTICS INTERNATIONAL LTD.	Livani Preilu Novads, LV

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016445722. Last updated year: 2026. Please use registration number 3016445722 when referencing this establishment in official correspondence.