FERRIS MFG. CORP.

FDA Device Registration & Listing · Fort Worth, TX, US · Registration 1419520

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
1419520
FEI Number
1419520
Entity Name
FERRIS MFG. CORP.
City/State/Country
Fort Worth, TX, US
Establishment Address
5133 Northeast Pkwy, Fort Worth, TX 76106, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
FERRIS MFG. CORP. (Owner Number: 1419520)
Owner / Operator Contact Address
5133 Northeast Parkway, --, Fort Worth, TX 76106, US
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
KMF Bandage, Liquid General Hospital Class 1 880.5090 2007-10-10
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2001-12-06
IPY Orthosis, Lumbo-Sacral Physical Medicine Class 1 890.3490 2002-01-02
FRO Dressing, Wound, Drug Unknown Class U N/A 2007-10-10
FRO Dressing, Wound, Drug Unknown Class U N/A 2007-10-10
NAD Dressing, Wound, Occlusive General, Plastic Surgery Class 1 878.4020 2025-01-28
KMF Bandage, Liquid General Hospital Class 1 880.5090 2007-10-10

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FERRIS MFG. 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
K150256 Argentum Medical SILVERLON BURN CONTACT DRESSINGS 2015-04-30
K881936 Iberhospitex, S.A. OPER-FILM-ADHESIVE MEMBRANE 1988-08-31

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
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 1419520. Last updated year: 2026. Please use registration number 1419520 when referencing this establishment in official correspondence.
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