LIFE SCIENCE PRODUCTS, INC.

FDA Device Registration & Listing · CHESTERTOWN, MD, US · Registration 3003823770

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
3003823770
FEI Number
3003823770
Entity Name
LIFE SCIENCE PRODUCTS, INC.
City/State/Country
CHESTERTOWN, MD, US
Establishment Address
124 Speer Rd, CHESTERTOWN, MD 21620, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
LIFE SCIENCE PRODUCTS, INC. (Owner Number: 9060767)
Owner / Operator Contact Address
124 Speer Road, --, Chestertown, MD 21620, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K101595
PMA Number
N/A

All Registered Proprietary Names

Sentinel Guardian - Latex Sentinel Guardian - Nitrile

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LYY Latex Patient Examination Glove General Hospital Class 1 880.6250 2023-08-30
LZA Polymer Patient Examination Glove General Hospital Class 1 880.6250 2023-08-30

Official Correspondent

Stevan Dodson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LIFE SCIENCE PRODUCTS, 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
K101595 Better Care Plastic Technology Cp., Ltd. POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE 2010-08-06
K894452 Kerala Rubber & Reclaims, Ltd. KRR GLOVE, PATIENT EXAMINATION GLOVES 1989-08-09
K891323 Li Wah-Hong Kong, Inc. LI WAH LATEX EXAMINATION GLOVES 1989-08-31
K891418 C & K Mfg. & Sales Co. LATEX EXAMINATION GLOVES, STYLE 510 LX 1989-06-22
K994255 Pt. Maja Agung Latexindo LATEX EXAMINATION GLOVES-PRE-POWDERED-STERILE 2000-02-07

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003823770. Last updated year: 2026. Please use registration number 3003823770 when referencing this establishment in official correspondence.
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