BioMed Laboratories, LLC.
FDA Regulatory Profile
BioMed Laboratories, LLC. appears in FDA public data with 1 recall, 1 510(k) clearance, 8 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-0663-2026, Class II) was initiated on June 11, 2026. Its most recent 510(k) clearance was granted on January 5, 2011.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 1
- Inspections
- 8
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| D-0663-2026 | Class II | Medline Remedy Specialized Silicone Cream (Hydraguard-D ),Manufactured for Medline Industries, LP, T | June 11, 2026 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K100613 | BIOMED WOUND CLEANSER | January 5, 2011 |