Data / Medical devices / United States / Life Science Products, Inc.
Life Science Products, Inc.: FDA-registered device maker in Chestertown, MD, United States, 3 510(k) clearances
Life Science Products, Inc. is registered with the FDA (registration 3003823770) in Chestertown, MD, United States. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated March 29, 2017. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3003823770
- Address
- 124 Speer Rd, Chestertown, MD, United States, 21620
- Owner or operator
- LIFE SCIENCE PRODUCTS, INC. (9060767)
- Roles
- Repackager or relabeler
- First device listed
- August 30, 2023
- Registered through
- 2027
- Brand names listed
- Sentinel Guardian - Latex, Sentinel Guardian - Nitrile
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Latex Patient Examination Glove | LYY | 1 | Repackager or relabeler | accessdata.fda.gov |
| Medical Glove, Specialty | LZC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Polymer Patient Examination Glove | LZA | 1 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 29, 2017 | K161929 | Palm-Pro Chemo-Guard Nitrile Powder Free Examination Glove | LZA | Substantially Equivalent | Dipped Products (Thailand) Limited | accessdata.fda.gov |
| August 6, 2010 | K101595 | POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE | LZA | Substantially Equivalent | Better Care Plastic Technology Cp., Ltd. | accessdata.fda.gov |
| October 11, 1996 | K953213 | COMFIT (POWDER FREE EXAMINATION GLOVES (HYPOALLERGENIC, LOW PROTEIN, BEADED) | LYY | Substantially Equivalent | Wembley Rubber Products (M) Sdn Bhd | accessdata.fda.gov |
Compare with other makers
- All makers of Polymer Patient Examination Glove
- All makers of Latex Patient Examination Glove
- All makers of Medical Glove, Specialty
Updated March 29, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.