Product code MEF
- Device name
- Ring, Teething, Non-Fluid Filled
- Medical specialty
- Dental
- Device class
- 1
- Regulation number
- 872.5550
- Review panel
- DE
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K034017 | JEJE TEETHER | Vibe 2000 | 2004-10-18 |
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| Primary DI | Brand | Company | Published |
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| 00049696898232 | B.PURE | FOURSTAR GROUP INC. | 2026-06-09 |
| 00049696198189 | B.PURE | FOURSTAR GROUP INC. | 2026-06-09 |
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