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Sign in to claim this brandQuasar Bio-Tech Inc
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 4588 PONDEROSA WAY, Yorba Linda, CA, 92886
- Website
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- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3006182559
- DUNS Number
- —
Catalogue (23)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Clear Rayz for Him WH | DPA-021-Him/WH | FDA UDI | Class II | Active |
| Quasar MD Blue Pink | DPA-022-PK | FDA UDI | Class II | Active |
| Pure Rayz for Him WH | DPA-026-Him/WH | FDA UDI | Class II | Active |
| Clear Rayz for Him Stormy | DPA-021-Stormy | FDA UDI | Class II | Active |
| Pure Rayz White | DPA-026-WH | FDA UDI | Class II | Active |
| Pure Rayz for Him - Sage | DPA-026-Sage | FDA UDI | Class II | Active |
| Quasar MD Plus | DPA-024 | FDA UDI | Class II | Active |
| Professional Red | DPA-004Red | FDA UDI | Class II | Active |
| Baby Quasar Plus | DPA-023 | FDA UDI | Class II | Active |
| Clear Rayz for Him Titanium | DPA-021-Titanium | FDA UDI | Class II | Active |
| Baby Quasar Plus Pink | DPA-023-PK | FDA UDI | Class II | Active |
| Professional Blue | DPA-006A | FDA UDI | Class II | Active |
| Baby Quasar Plus 14K | DPA-023-Gold | FDA UDI | Class II | Active |
| Pure Rayz for Him - Reflecting | DPA-026-Reflecting | FDA UDI | Class II | Active |
| Pure Rayz for Him Frost | DPA-026-Frost | FDA UDI | Class II | Active |
| Quasar MD Blue | DPA-022 | FDA UDI | Class II | Active |
| Quasar MD Plus Pink | DPA-024-PK | FDA UDI | Class II | Active |
| Baby Blue Pink | DPA-002-PK | FDA UDI | Class II | Active |
| Baby Blue | DPA-002 | FDA UDI | Class II | Active |
| Pure Rayz Teal | DPA-026-PRTEAL | FDA UDI | Class II | Active |
| Pure Rayz Pink | DPA-026-PRPK | FDA UDI | Class II | Active |
| Baby Quasar Plus Teal | DPA-023-Teal | FDA UDI | Class II | Active |
| Healing Rayz | DPA-027 | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (3)
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 |
|---|---|---|---|---|
| Jun 29, 2018 | Z-2974-2018 | — | terminated | Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals. |
| Jun 29, 2018 | Z-2975-2018 | — | terminated | Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals. |
| Jun 29, 2018 | Z-2973-2018 | — | terminated | Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals. |