4 MED LTD.

FDA Device Registration & Listing · Nahal-Oz Southern, IL · Registration 3004135030

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004135030
FEI Number
3004135030
Entity Name
4 MED LTD.
City/State/Country
Nahal-Oz Southern, IL
Establishment Address
Nahal-Oz, 1, Nahal-Oz Southern 8514500, IL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
4 MED LTD. (Owner Number: 9058303)
Owner / Operator Contact Address
16 SHIVAT ZION STREET, --, KFAR SAVA, IL-NOTA 44286, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dermatome Blades SKIN GRAFT KNIFE BLADE "Rosenberg" Skin Graft Mesher "Rosenberg" Variable Mesher Rosenberg Mouth Gag SKIN GRAFT CARRIER "Rosenberg" Deramtoms SKIN GRAFT KNIFE OCCLUDRESS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GES Blade, Scalpel General, Plastic Surgery Class 1 878.4800 2007-01-25
FZW Expander, Surgical, Skin Graft General, Plastic Surgery Class 1 878.4800 2005-05-18
KBN Gag, Mouth Ear, Nose, Throat Class 1 874.4420 2005-05-18
GEJ Carrier, Ligature General, Plastic Surgery Class 1 878.4800 2007-01-25
EMF Knife, Surgical General, Plastic Surgery Class 1 878.4800 2005-05-18
NAD Dressing, Wound, Occlusive General, Plastic Surgery Class 1 878.4020 2007-02-28

Official Correspondent

No official correspondent registered.

US Agent Details

Mark Sherrard Business: Sherrard and Associates LLC Email: sales@4med-surgical.com Phone: (914) 8610480

Related Public Records

Same Entity

4 MED LTD.
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
K881936 Iberhospitex, S.A. OPER-FILM-ADHESIVE MEMBRANE 1988-08-31

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0012-2008 Becton Dickinson & Company 1
Shelf Pack: Bard-Parker Rib-Back Carbon Steel no.11, surgical blade. Unit Package: Contents of unopened or undamaged package guaranteed sterile; After use place product in a puncture resistant container and dispose properly. Becton Dickinson Becton Dickinson Acute Care Franklin Lakes, NJ 07417
Z-0013-2008 Becton Dickinson & Company 1
Shelf Pack: Bard-Parker Rib-Back Stainless Steel no.11, surgical blade. Unit Package: Contents of unopened or undamaged package guaranteed sterile; After use place product in a puncture resistant container and dispose properly. Becton Dickinson Becton Dickinson Acute Care Franklin Lakes, NJ 07417
Z-0013-2019 COVIDIEN LLC 1
Kerlix AMD Antimicrobial Bandage Roll, 6 Ply, 4-1/2 x 12.3 (11.4 cm x 3.7m), REF 3332 Product Usage- as both primary and secondary dressing containing PHMB (polyhexamethylene biguanide) to resist bacterial colonization within the dressing and bacterial penetration through the dressing.
Z-0014-2019 COVIDIEN LLC 1
Kerlix Bandage Roll, 100% Cotton, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m), REF 6715 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0015-2019 COVIDIEN LLC 1
Kerlix Gauze Roll, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m) Stretched, REF 7880 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004135030. Last updated year: 2026. Please use registration number 3004135030 when referencing this establishment in official correspondence.
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