Data / Medical devices / United States / Wells Lamont Industrial, LLC
Wells Lamont Industrial, LLC: FDA-registered device maker in Philadelphia, MS, United States, 3 510(k) clearances
Wells Lamont Industrial, LLC is registered with the FDA (registration 3011592859) in Philadelphia, MS, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 10, 1995. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3011592859
- Address
- 299A W Beacon St, Philadelphia, MS, United States, 39350
- Owner or operator
- WELLS LAMONT INDUSTRIAL (9002369)
- Roles
- Manufacturer
- First device listed
- April 8, 1994
- Registered through
- 2027
- Brand names listed
- Sterile Product-2, Sterile Product-3, Sterile Product-4, Sterile-1, Sterile-2
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Manufacturer | accessdata.fda.gov |
| Sheet, Burn | FPY | 1 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| April 10, 1995 | K944763 | CUT-TEC OR WELLS LAMONT POLYESTER/WIRE CUT-RESISTANT GLOVE LINER WELLS-TEC, SCEPTER | LYU | Substantially Equivalent | Wells Lamont Corp. | accessdata.fda.gov |
| May 12, 1994 | K940274 | NYLON LINER GLOVES | LYU | Substantially Equivalent | Wells Lamont Corp. | accessdata.fda.gov |
| June 15, 1993 | K922407 | WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS | LYU | Substantially Equivalent | Wells Lamont Corp. | accessdata.fda.gov |
Compare with other makers
Updated April 10, 1995. 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.