Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1932902

FEI Number

1000158435

Entity Name

CERTIFIED SAFETY MFG., INC.

City/State/Country

KANSAS CITY, MO, US

Establishment Address

1400 Chestnut Ave, KANSAS CITY, MO 64127, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

CERTIFIED SAFETY MFG., INC. (Owner Number: 9010174)

Owner / Operator Contact Address

1400 CHESTNUT, --, Kansas City, MO 64127, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Eye Pad Certi-Gauze Non-Stick Pad, 2" x 3" Certi-Stopper XLG Trauma Dressing Trauma Kits Trauma Pad, 5 Burn Trauma Kit, 16 and 24 Unit Certi-Gauze Compress 36" X 36" Certi-Gauze Compress 18" X 36" Certi-Gauze Compress 24" X 72" Certi-Gauze Roll, 4" X 6 yd. Certi-Gauze Roll, 2" X 6 yd. Certi-Strip

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HMP	Pad, Eye	General, Plastic Surgery	Class 1	878.4440	2007-11-13
EFQ	Gauze/Sponge, Internal	Unknown	Class U	N/A	2007-11-13
EFQ	Gauze/Sponge, Internal	Unknown	Class U	N/A	2007-11-13
LRR	First Aid Kit With Drug	Unknown	Class N	N/A	2007-11-13
EFQ	Gauze/Sponge, Internal	Unknown	Class U	N/A	2007-11-13
LRR	First Aid Kit With Drug	Unknown	Class N	N/A	2007-11-13
EFQ	Gauze/Sponge, Internal	Unknown	Class U	N/A	2007-11-13
EFQ	Gauze/Sponge, Internal	Unknown	Class U	N/A	2007-11-13
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2009-07-28

Official Correspondent

PAM GERSON

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CERTIFIED SAFETY MFG., INC.

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
K861444	Surgical Specialties, Inc.	S1 NASAL PACKING	1986-05-06
K863737	Hermitage Hospital Products, Inc.	SPONGES STERILE TWIN PAKT AND SINGLES	1986-10-14
K940351	Certified Safety Mfg., Inc.	EXTRA LARGE COMPRESS DRESSING	1994-02-25
K950404	Lockett Medical Corp.	LOCKETT MEDICAL CORP. GAUZE	1995-04-17
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21

Similar Registrations

Registration Number	Establishment Name	Location
3045061271	YANGZHOU HUANRUI MEDICAL TECHNOLOGY CO., LTD	Baoying County Jiangsu, CN
3014819517	WELLMIEN HEALTHCARE TECH.(SUZHOU) CO., LTD.	Suzhou Jiangsu, CN
1422634	MEDLINE INDUSTRIES, LP (Northpoint Services)	Waukegan, IL, US
3012865799	NEOMED CO., LTD.	Saha-gu Busan, KR
3045030500	HEFEI BAOGUO INFORMATION TECHNOLOGY CO., LTD	Hefei Anhui, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1932902. Last updated year: 2026. Please use registration number 1932902 when referencing this establishment in official correspondence.