Endoch EAI-0782
by Endoch Inc
Endoch EAI-0782 is a Class II device made by Endoch Inc, cleared under FDA 510(k) K171825 on 13 Feb 2018 and listed in FDA GUDID since 1 Jun 2019 (UDI-DI EAI0782), 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 | NumberEAI0782 | Date1 Jun 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK171825 | Date13 Feb 2018 | StatusActive |
Official records
- FDA 510(k) database K171825
Across registries
- FDA 510(k) K171825 decided 13 Feb 2018 Active
- FDA GUDID UDI-DI EAI0782 listed 1 Jun 2019 Listed
Timeline
- Cleared FDA 510(k) K171825
- Listed FDA GUDID EAI0782
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Endoch
- Generic name
- Rigid endoscopic scissors, single-use
- Model / Ref / Catalog
- EAI-0782
- Primary DI / UDI-DI
- EAI0782
- 510(k) Number
- FDA product code
- GEI, JOK
- GMDN term
- Rigid endoscopic scissors, single-use
- Device class
- Class II
- Regulation number
- 878.4400, 880.6820
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories).
- Enseal NSLG2S35A by Ethicon Endo-Surgery, LLC
- Rita Systems by Rita Medical Systems, Inc.
- DENSITY; DENZA; DENSITY Noir by Jeisys Medical Incorporated
- Guenter Bissinger Medizintechnik GmbH 81528341 by Günter Bissinger Medizintechnik GmbH
- ERBE 20189-352 by Erbe Elektromedizin GmbH
- On-Gard Cord-Caddy by On-Gard Systems, Inc.
- Model 8700 Bipolar Electrosurgical Generator by Everest Medical Corp.
- Gimmi Z.5536.30 by Gimmi GmbH
- triFX GEN 36L by POLLOGEN LTD
- Morpheus8 Burst Deep Applicator AG613056A by Inmode MD, Ltd.