Data / Medical devices / United States / Happiest Baby, Inc.
Happiest Baby, Inc.: FDA-registered device maker in Los Angeles, CA, United States, 1 510(k) clearance
Happiest Baby, Inc. is registered with the FDA (registration 3030187577) in Los Angeles, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 30, 2023. 2 recall events name it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030187577
- Address
- 11390 W Olympic Blvd. Suite 450, Los Angeles, CA, United States, 90064
- Owner or operator
- Happiest Baby, Inc. (10089516)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- December 27, 2023
- Registered through
- 2026
- Brand names listed
- SNOO Smart Sleeper
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Infant Supine Sleep System | QTG | 2 | Complaint file establishment, Specification developer | 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 |
|---|---|---|---|---|---|---|
| March 30, 2023 | DEN210039 | SNOO Smart Sleeper | QTG | Unknown | Happiest Baby, Inc. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| August 7, 2026 | 99608 | Class II | Ongoing | Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101 S2107-110 | Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA. | accessdata.fda.gov |
| May 15, 2024 | 99365 | Class II | Ongoing | Happiest Baby, Inc Pre-loved SNOO Smart Sleeper Model:S1000 | This recall is retroactively being reported. Refurbished bassinets failed to meet quality standards prior to distribution. | accessdata.fda.gov |
Compare with other makers
Updated September 15, 2026. 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.