Data / Medical devices / United States / Alumni Partners
Alumni Partners: FDA-registered device maker in San Clemente, CA, United States, 1 510(k) clearance
Alumni Partners is registered with the FDA (registration 3011835632) in San Clemente, CA, United States. It lists 8 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 20, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011835632
- Address
- 140 Calle Iglesia, San Clemente, CA, United States, 92672
- Owner or operator
- Alumni Partners (10053316)
- Roles
- Repackager or relabeler
- First device listed
- November 23, 2016
- Registered through
- 2026
- Brand names listed
- Alcohol Wipe, Bead Therapy, CPP-5466, CPP-7725, CPP-7832, CPP-7837, CPR FACE SHIELD, Chic Sunglasses and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Repackager or relabeler | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Repackager or relabeler | accessdata.fda.gov |
| Mask, Scavenging | KHA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Mouthpiece, Breathing | BYP | 1 | Repackager or relabeler | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | Repackager or relabeler | accessdata.fda.gov |
| Pad, Alcohol, Device Disinfectant | LKB | U | Repackager or relabeler | accessdata.fda.gov |
| Sunglasses (Non-Prescription Including Photosensitive) | HQY | 1 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| November 20, 2018 | K182133 | Infrared Thermometer | FLL | Substantially Equivalent | Shenzhen AOJ Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Accessory, Surgical Apparel
- All makers of Mask, Scavenging
- All makers of Pad, Alcohol, Device Disinfectant
- All makers of Pack, Hot Or Cold, Reusable
- All makers of Mouthpiece, Breathing
- All makers of Massager, Therapeutic, Electric
Updated November 20, 2018. 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.