KERICURE MEDICAL

FDA Device Registration & Listing · Land O Lakes, FL, US · Registration 3010131715

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
3010131715
FEI Number
3010131715
Entity Name
KERICURE MEDICAL
City/State/Country
Land O Lakes, FL, US
Establishment Address
24327 Oaks Blvd, Land O Lakes, FL 34639, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
KeriCure Medical (Owner Number: 10043631)
Owner / Operator Contact Address
24327 Oaks Blvd, Land O Lakes, FL 34639, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Field Shield Hydrogel Wound Dressing Field Shield Wound Dressing Field Shield PRO Wound Dressing Natural Shield Silver First Aid Advanced Shield MAX Wound Barrier Advanced Shield Chronic Wound Barrier Advanced Shield Hydrogel Wound Barrier Advanced Seal Wound Barrier

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRO Dressing, Wound, Drug Unknown Class U N/A 2024-07-31
NEC Bandage, Liquid, Skin Protectant General Hospital Class 1 880.5090 2013-03-06
NAE Dressing, Wound, Hydrogel Without Drug And/Or Biologic General, Plastic Surgery Class 1 878.4022 2020-03-28

Official Correspondent

Kerriann Greenhalgh

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KeriCure Medical
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
K150256 Argentum Medical SILVERLON BURN CONTACT DRESSINGS 2015-04-30

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0003-06 B. Braun Medical, Inc. U
D-Stat Dry Hemostatic Bandage. The product is an adhesive bandage.
Z-0038-2025 3M Company Health Care Business 3m Center U
3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R

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3012456427 UFP TECHNOLOGIES, INC. Newburyport, MA, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010131715. Last updated year: 2026. Please use registration number 3010131715 when referencing this establishment in official correspondence.
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