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Sign in to claim this brandAdler MicroMed, Inc.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 6842 Elaine Way, San Diego, CA, 92120
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3011412640
- DUNS Number
- —
Catalogue (19)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Adler MicroMed Laser Surgery Fiber | BFCS000233 | FDA UDI | Class II | Active |
| Adler MicroMed Laser Surgery Fiber | 631000304 | FDA UDI | Class II | Active |
| Adler MircroMed Laser Surgery Fiber | BFCS000288 | FDA UDI | Class II | Unknown |
| Adler MicroMed Laser Surgery Fiber | 631000302 | FDA UDI | Class II | Active |
| Adler MicroMed Laser Surgery Fiber | 635000235 | FDA UDI | Class II | Active |
| Adler MicroMed Laser Surgery Fiber | BFCS000304 | FDA UDI | Class II | Active |
| Adler MicroMed Laser Surgery Fiber | BFCS000302 | FDA UDI | Class II | Unknown |
| Adler MicroMed Laser Surgery Fiber | BFCS000296 | FDA UDI | Class II | Active |
| Adler MicroMed Laser Surgery Fiber | SFCS000235 | FDA UDI | Class II | Unknown |
| Adler Hemorrhoid Ligator | Adler Hemorrhoid Ligator | FDA UDI | Class II | Active |
| Hemorrhoid Ligator | AL8000 | FDA UDI | Class II | Unknown |
| Adler MicroMed Laser Surgery Fiber | SFCS000145 | FDA UDI | Class II | Active |
| Adler MicroMed Laster Surgery Fiber | SFCS000101 | FDA UDI | Class II | Active |
| Adler MicroMed Laser Surgery Fiber | 636000099 | FDA UDI | Class II | Active |
| Adler MicroMed Laser Surgery Fiber | SFCS000099 | FDA UDI | Class II | Unknown |
| Adler MicroMed Laser Surgery Fiber | 631000296 | FDA UDI | Class II | Active |
| Adler MicroMed Laser Surgery Fiber | 631000288 | FDA UDI | Class II | Active |
| Adler MicroMed Laser Surgery Fiber | SFCS000102 | FDA UDI | Class II | Active |
| Adler MicroMed Laser Surgery Fibers | K152417 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
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Importers
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Notified Bodies
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Authorities
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Apr 23, 2021 | Z-1901-2021 | — | terminated | Due to issue with product sterility. Sterilization service provider had falsified records. |