Dornier MedTech Medilas D FlexiPulse (D-Plug)
Dornier MedTech Medilas D FlexiPulse (D-Plug) (K2011743) is a Class II device made by Dornier MedTech GmbH, cleared under FDA 510(k) K070536 on 21 May 2007 and listed in FDA GUDID since 11 Sep 2018 (UDI-DI 04049958001307), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04049958001307 | Date11 Sep 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK070536 | Date21 May 2007 | StatusActive |
Official records
- AccessGUDID record 04049958001307
- FDA 510(k) database K070536
Across registries
- FDA 510(k) K070536 decided 21 May 2007 Active
- FDA GUDID UDI-DI 04049958001307 listed 11 Sep 2018 Listed
Timeline
- Cleared FDA 510(k) K070536
- Listed FDA GUDID 04049958001307
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Dornier MedTech
- Generic name
- General/multiple surgical diode laser system
- Model / Ref / Catalog
- Medilas D FlexiPulse (D-Plug), K2011743
- Primary DI / UDI-DI
- 04049958001307
- 510(k) Number
- FDA product code
- GEX
- GMDN term
- General/multiple surgical diode laser system
- Device class
- Class II
- Regulation number
- 878.4810
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under General/multiple surgical diode laser system.