Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003884600

FEI Number

3003884600

Entity Name

PAVIS S.P.A.

City/State/Country

Buguggiate Varese, IT

Establishment Address

Via Rossini 11b, Buguggiate Varese 21020, IT

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Pavis S.p.a. (Owner Number: 10057184)

Owner / Operator Contact Address

Via Rossini 11b, Buguggiate, IT-VA 21020, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ERNIABOXER SILVY ERNIABLOCK LADY SERVOCLIN LETIZIA ERNIABLOCK ELASTIC CALF SUPPORT PATELLA AND MCL-LCL STABILIZER WITH HOLE ADJUSTABLE ELASTIC KNEE BRACE WITH HOLE AND POLYCENTRIC STAYS ACL-PCL AND MCL-LCL INSTABILITY BRACE PATELLA STABILIZER KNEE BRACE FOR LIGHT MCL-LCL INSTABILITY THIGH WRAP WITH PAD JUMPER'S KNEE BRACE ADJUSTABLE ELASTIC KNEE WRAP TUBE-SHAPED KNEE BRACE WITH HOLE STOD POSTURE TRAINER SELF-CARE+ BACK BRACE LUMBOSACRAL BRACE HIGH LUMBOSACRAL BRACE LOW WITH THERMOFORMABLE PANEL LIGHT LUMBAR BELT SELF-CARE LUMBOSACRAL BRACE HIGH WITH THERMOFORMABLE PANEL LUMBOSACRAL BRACE LOW ORTHO-E BACK BRACE DORSAL-LUMBO-SACRAL MODULAR CORSET

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EXN	Support, Hernia	Gastroenterology, Urology	Class 1	876.5970	2018-03-05
ITQ	Joint, Knee, External Brace	Physical Medicine	Class 1	890.3475	2023-03-31
IQE	Orthosis, Lumbar	Physical Medicine	Class 1	890.3490	2023-03-31

Official Correspondent

Barbara Frangi

US Agent Details

Emily Matorin Email: usagent@fdabasics.com Phone: (716) 7750533

Related Public Records

Same Entity

Pavis S.p.a.

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 3003884600. Last updated year: 2026. Please use registration number 3003884600 when referencing this establishment in official correspondence.