Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020983482

FEI Number

3020983482

Entity Name

UNISIS CORP

City/State/Country

Kita-Hiroshima-shi Hokkaido, JP

Establishment Address

1-2-8 Wattsu Industrial Complex, Kita-Hiroshima-shi Hokkaido 061-1281, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Unisis Corp (Owner Number: 10083347)

Owner / Operator Contact Address

1-2-8 Wattsu Industrial Complex, Kita-Hiroshima-shi, JP-01 061-1281, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K141126

PMA Number

N/A

All Registered Proprietary Names

Uniever Disposable Nerve Blockade Needle Uniever Disposable Epidural Anesthesia Needle Uniever Disposable Spinal Anesthesia Needle

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MIA	Needle, Spinal, Short Term	Anesthesiology	Class 2	868.5150	2024-12-26
LRO	General Surgery Tray	General, Plastic Surgery	Class 2	878.4370	2021-12-13
MIA	Needle, Spinal, Short Term	Anesthesiology	Class 2	868.5150	2024-12-26
BSP	Needle, Conduction, Anesthetic (W/Wo Introducer)	Anesthesiology	Class 2	868.5150	2024-12-26
BSP	Needle, Conduction, Anesthetic (W/Wo Introducer)	Anesthesiology	Class 2	868.5150	2021-12-13
BSP	Needle, Conduction, Anesthetic (W/Wo Introducer)	Anesthesiology	Class 2	868.5150	2024-12-26
BSP	Needle, Conduction, Anesthetic (W/Wo Introducer)	Anesthesiology	Class 2	868.5150	2021-11-12
BSP	Needle, Conduction, Anesthetic (W/Wo Introducer)	Anesthesiology	Class 2	868.5150	2021-11-12

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Unisis Corp

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
K961683	J.J. Skinner, Inc.	JJ SKINNER CAREKITS MINOR SURGICAL PROCEDURE TRAY	1996-05-10

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2025	Windstone Medical Packaging, Inc.	2	Aligned Medical Tonsil Tray REF AMS9300A that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a convenient manner for use in a general clinical procedure.
Z-0028-2025	Windstone Medical Packaging, Inc.	2	Aligned Medical Tonsil ENT Pack REF AMS9977 that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a convenient manner for use in a general clinical procedure.
Z-0030-2025	Windstone Medical Packaging, Inc.	2	Aligned Medical T and A Pack REF AMS11482 that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a convenient manner for use in a general clinical procedure.
Z-0031-2025	Windstone Medical Packaging, Inc.	2	Aligned Medical Tonsil Pack REF AMS14809 that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a convenient manner for use in a general clinical procedure.
Z-0095-2021	Alcon Research, LLC	2	Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health" PROTEXIS" Latex Micro Surgical Gloves - Product Usage: used by ophthalmic surgeons in a variety of ophthalmic surgeries.

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3035642068	Honduras Kitting, S.A.	Villanueva Cortes, HN
1224960	SPECTRA MEDICAL DEVICES, LLC	WILMINGTON, MA, US
1316297	EPIMED INTERNATIONAL, INC.	JOHNSTOWN, NY, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020983482. Last updated year: 2026. Please use registration number 3020983482 when referencing this establishment in official correspondence.