Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016010820

FEI Number

3016010820

Entity Name

V SOFT LIFT AB

City/State/Country

Skogas Stockholm, SE

Establishment Address

Lyftkransvagen 7A, Skogas Stockholm 142 50, SE

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Foreign Private Label Distributor

Owner / Operator

V Soft Lift AB (Owner Number: 10061710)

Owner / Operator Contact Address

Lyftkransvagen 7A, Skogas, SE-AB 14250, SE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K172602

PMA Number

N/A

All Registered Proprietary Names

V SOFT LINE BARB STAR 21Gx90mm V SOFT LINE BARB BLUNT CANNULA 23Gx60mm V SOFT LINE ARTE 18Gx100mm V SOFT LINE BARB BLUNT CANNULA L 21Gx90mm V SOFT LINE ARTE2 19Gx100mm V SOFT LINE ARTE2 18Gx100mm V SOFT LINE ARTE3 17GGx100mm V SOFT LINE BARB BLUNT CANNULA L 4D 21Gx60mm V SOFT LINE BARB STAR 19Gx90mm V SOFT LINE ARTE3 17GGx70mm V SOFT LINE FN NETFILL 21Gx60mm V SOFT LINE ARTE 19Gx100mm V SOFT LINE BARB STAR 21Gx60mm V SOFT LINE FN NETFILL 21Gx30mm V SOFT LINE BARB Blunt Cannula N 19Gx100mm V SOFT LINE BARB BLUNT CANNULA L 21Gx60mm V SOFT LINE BARB BLUNT CANNULA L 4D 21Gx90mm V SOFT LINE BARB Blunt Cannula L 19Gx40mm V SOFT LINE BI BARBED FCN BI 19Gx100mm V SOFT LINE FN NETFILL 21Gx45mm

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NEW	Suture, Surgical, Absorbable, Polydioxanone	General, Plastic Surgery	Class 2	878.4840	2019-11-12

Official Correspondent

Martin Richter

US Agent Details

Jacob Gruenebaum Business: SDAB Partners Email: jacob@vsoftlift.us Phone: (800) 6749640

Related Public Records

Same Entity

V Soft Lift AB

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016010820. Last updated year: 2026. Please use registration number 3016010820 when referencing this establishment in official correspondence.