Is this your brand? Sign in to claim ownership.
Sign in to claim this brandLuv N' Care, Ltd.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 3030 Aurora Ave FL 2nd, Monroe, LA, 71201
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 2381321
- DUNS Number
- 108926288
Catalogue (28)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nuby | 671 | FDA UDI | Class II | Active |
| Nuby | 6921 | FDA UDI | Class II | Active |
| Nuby | 81191 | FDA UDI | Class I | Active |
| Nuby | 6884 | FDA UDI | Class II | Active |
| Nuby | 92419 | FDA UDI | Class II | Active |
| Nuby | 81177 | FDA UDI | Class II | Active |
| Nuby | 624 | FDA UDI | Class II | Active |
| Nuby | 633 | FDA UDI | Class II | Active |
| Nuby | 6648 | FDA UDI | Class II | Active |
| Nuby | 768 | FDA UDI | Class I | Active |
| Nuby | 80274 | FDA UDI | Class I | Active |
| Nuby | 6938 | FDA UDI | Class II | Active |
| Always My Baby | 16449 | FDA UDI | Class II | Active |
| Nuby | 567 | FDA UDI | Class II | Active |
| Nuby | 602 | FDA UDI | Class II | Active |
| Nuby | 509 | FDA UDI | Class II | Active |
| Nuby | 80275 | FDA UDI | Class I | Active |
| Nuby | 80276 | FDA UDI | Class I | Active |
| Nuby | 6937 | FDA UDI | Class II | Active |
| Nuby | 621 | FDA UDI | Class II | Active |
| Nuby | 49196 | FDA UDI | Class II | Active |
| Nuby | 719 | FDA UDI | Class II | Active |
| Nuby | 6909 | FDA UDI | Class II | Active |
| Nuby | 601 | FDA UDI | Class II | Active |
| Nuby | 625 | FDA UDI | Class II | Active |
| Nuby | 600 | FDA UDI | Class II | Active |
| Nuby Natural Touch Rhythm Dual Action Electric Breast Pump | K100385 | FDA 510(k) | Class II | Active |
| Gel Filled Gum Soother | K092494 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
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 |
|---|---|---|---|---|
| Jul 17, 2009 | Z-1878-2009 | — | terminated | Gel filled teethers were found to contain to contain Bacillus circulans and Bacillus subtilis. |