Data / Medical devices / France / LPG Systems
LPG Systems: FDA-registered device maker in VALENCE Drome, France, 2 510(k) clearances
LPG Systems is registered with the FDA (registration 3003454229) in VALENCE Drome, France. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 6, 2006. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3003454229
- Address
- 30 Rue Du Docteur Abel, VALENCE Drome, France, 26902
- Owner or operator
- LPG SYSTEMS (9031161)
- Roles
- Manufacturer, Specification developer
- First device listed
- March 5, 1999
- Registered through
- 2027
- Brand names listed
- Cellu M6 Alliance Lab Medical, Cellu M6 Alliance Medical, Cellu M6 Endermolab 2i, Cellu M6 Endermolab i, Cellu M6 Infinity, Cellu M6 Integral 2i, Cellu M6 Integral i, CelluM6 Endermolab 2i and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Exerciser, Powered | BXB | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| System, Isokinetic Testing And Evaluation | IKK | 2 | Specification developer | accessdata.fda.gov |
| Vibrator, Therapeutic | IRO | 1 | Manufacturer, 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 |
|---|---|---|---|---|---|---|
| November 6, 2006 | K053225 | CELLU M6 KEYMODULE I | ISA | Substantially Equivalent | Lpg One, Inc. | accessdata.fda.gov |
| January 18, 2000 | K990445 | LPG THERAPEUTIC MASSAGER, MODELS -ESI, THERAPEUTIC MASSAGER/VIBRATOR | ISA | Substantially Equivalent | Lpg USA, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Massager, Therapeutic, Electric
- All makers of System, Isokinetic Testing And Evaluation
- All makers of Vibrator, Therapeutic
- All makers of Exerciser, Powered
Updated November 6, 2006. 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.