Fmx G1FP
Fmx G1FP (FMG1FP) is a Class II device made by Domain Surgical, Inc., cleared under FDA 510(k) K110439 on 18 Jul 2011 and listed in FDA GUDID since 8 Jun 2016 (UDI-DI 00859729006035), 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 | GUDID listing | Number00859729006035 | Date8 Jun 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK110439 | Date18 Jul 2011 | StatusActive |
Official records
- AccessGUDID record 00859729006035
- FDA 510(k) database K110439
Across registries
- FDA 510(k) K110439 decided 18 Jul 2011 Active
- FDA GUDID UDI-DI 00859729006035 listed 8 Jun 2016 Listed
Timeline
- Cleared FDA 510(k) K110439
- Listed FDA GUDID 00859729006035
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Fmx
- Generic name
- Foot-switch, electrical
- Model / Ref / Catalog
- G1FP, FMG1FP
- Primary DI / UDI-DI
- 00859729006035
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Foot-switch, electrical
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Foot-switch, electrical.
- CannulaCRF CRF-C1030 by Cambridge Interventional LLC
- Electrosurgical Unit ZEUS PRIME by Zerone Co., Ltd.
- ElectrodeCRF CRF-U1030 by Cambridge Interventional LLC
- Cool-tip RFASW by Covidien LP
- Dophi SJ-A01 by Surgnova Healthcare Technologies (Zhejiang) Co., Ltd.
- Valleylab E6008L by Covidien LP
- ERBE 20188-350 by Erbe Elektromedizin GmbH
- ERBE 20188-102 by Erbe Elektromedizin GmbH
- LEKTRAFUSE GN201 by AESCULAP, INC.
- VASER 115-0011 by Solta Medical, Inc.