Md-Flex Heavy Body
510(k) K134008
Md-Flex Heavy Body is a Class II device made by Meta Biomed, Inc., cleared under FDA 510(k) K134008 on 9 Apr 2014, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK134008 | Date9 Apr 2014 | StatusActive |
Official records
- FDA 510(k) database K134008
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- ELW
- Device class
- Class II
- Regulation
- 21 CFR Part 872.3660
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K134008
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| MD Flex heaby body 9284 | 9284 | 08806387892847 | — | No longer on the market |
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