Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9617977

FEI Number

3002535141

Entity Name

KENCAP LTD.

City/State/Country

Savyon Southern, IL

Establishment Address

West Milford Nj 07480, 9, Ha-Mitnakhalim, Savyon Southern 5690500, IL

Establishment Type(s)

Repack or Relabel Medical Device,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

KENCAP LTD. (Owner Number: 9033765)

Owner / Operator Contact Address

1614-0 Union Valley Road, Suite 112, West Milford, NJ 07480, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

EARDOC KENCAP,

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KDD	Kit, Surgical Instrument, Disposable	General, Plastic Surgery	Class 1	878.4800	1998-05-06

Official Correspondent

No official correspondent registered.

US Agent Details

Doreen Hamaoui Business: PHD-TAX Email: D@phd-tax.com Phone: (425) 6792036

Related Public Records

Same Entity

KENCAP LTD.

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 9617977. Last updated year: 2026. Please use registration number 9617977 when referencing this establishment in official correspondence.