Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1925025

FEI Number

1000118065

Entity Name

LIGHTHOUSE FOR THE BLIND

City/State/Country

Saint Louis, MO, US

Establishment Address

10440 TRENTON AVE., Saint Louis, MO 63132, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

LIGHTHOUSE FOR THE BLIND (Owner Number: 9004139)

Owner / Operator Contact Address

10440 TRENTON AVE., --, Saint Louis, MO 63132, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K043063

PMA Number

N/A

All Registered Proprietary Names

UltraFlex No Proprietary Name Oxyband

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KOA	Surgical Instruments, G-U, Manual (And Accessories)	Gastroenterology, Urology	Class 1	876.4730	2013-01-18
OKH	Body Fluids Barrier Kit	General, Plastic Surgery	Class 2	878.4040	2012-01-23
IMD	Pack, Hot Or Cold, Disposable	Physical Medicine	Class 1	890.5710	2013-01-18
OHO	First Aid Kit Without Drug	General, Plastic Surgery	Class 1	878.4014	2011-05-05
NAD	Dressing, Wound, Occlusive	General, Plastic Surgery	Class 1	878.4020	2012-08-20

Official Correspondent

Scott Lemmons

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LIGHTHOUSE FOR THE BLIND

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
K880871	John Wagner Associates, Inc.	GRABBER WARM PACK/MINI MINI HEATER/FOOT HEATER	1988-05-20
K881936	Iberhospitex, S.A.	OPER-FILM-ADHESIVE MEMBRANE	1988-08-31

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0505-2022	Philips North America Llc	1	Infa-Therm Transport Mattress, Reference Number 989805616831 1015
Z-0506-2022	Philips North America Llc	1	Infant Heel Warmers w/strap, Reference # 989805603201 1223
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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3009888344	Isomedix Operations Inc	El Paso, TX, US
3006082230	C.R. BARD, INC.	MADISON, GA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1925025. Last updated year: 2026. Please use registration number 1925025 when referencing this establishment in official correspondence.