BEAR MEDIC CORPORATION

FDA Device Registration & Listing · Daigomachi, Kuji-gun Ibaraki, JP · Registration 3007074233

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
3007074233
FEI Number
3007074233
Entity Name
BEAR MEDIC CORPORATION
City/State/Country
Daigomachi, Kuji-gun Ibaraki, JP
Establishment Address
1361 Daigo, Daigomachi, Kuji-gun Ibaraki 319-3526, JP
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Bear Medic Corporation (Owner Number: 10026011)
Owner / Operator Contact Address
1361 Daigo, Daigo-Machi, Kuji=gun, JP-08 319-3526, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAR Suture, Nonabsorbable, Synthetic, Polyamide General, Plastic Surgery Class 2 878.5020 2008-05-29
DXC Clamp, Vascular Cardiovascular Class 2 870.4450 2019-03-26
DXC Clamp, Vascular Cardiovascular Class 2 870.4450 2008-05-29

Official Correspondent

Fred Phelps

US Agent Details

Robyn Scopis Business: Regulatory Specialists Email: robyn@regulatoryspecialists.com Phone: (949) 2620411

Related Public Records

Same Entity

Bear Medic Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0034-2009 Surgical Specialties Corp 2
3-0 Black Mono Nylon Suture, 12 units per box. product number 925B. The product intended for use in general soft tissue approximation and/or ligation including use in ophthalmic procedures.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007074233. Last updated year: 2026. Please use registration number 3007074233 when referencing this establishment in official correspondence.
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