Allied Biomedical Corp.
Allied Biomedical Corp. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 5, 1998.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K982051 | KELOCATE SHEETING | August 5, 1998 |
| K971478 | DURALASTIC ANATOMICAL CHIN IMPLANTS | July 18, 1997 |
| K971479 | DURALASTIC ANATOMICAL MALAR IMPLANTS | July 18, 1997 |
| K971481 | DURALASTIC ANATOMICAL NASAL IMPLANTS | July 18, 1997 |
| K971480 | DURALASTIC I AND DURALASTIC II | May 28, 1997 |
| K955370 | DURALASTIC II | February 8, 1996 |
| K955368 | DURALASTIC I | February 8, 1996 |
| K955433 | DURALASTIC SILICONE TUBING | January 26, 1996 |
| K954413 | KELOCOTE | November 29, 1995 |