Data / Medical devices / Endoscopic Grasping/Cutting Instrument, Non-Powered / United States
FDA-registered makers of Endoscopic Grasping/Cutting Instrument, Non-Powered in the United States: 14 establishments
14 establishments in the United States are registered with the FDA to make Endoscopic Grasping/Cutting Instrument, Non-Powered (product code OCZ). 11 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.
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- Device
- Endoscopic Grasping/Cutting Instrument, Non-Powered
- Product code
- OCZ
- Country
- United States
Makers of Endoscopic Grasping/Cutting Instrument, Non-Powered in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Avanos Medical, Inc. | Alpharetta, GA, United States | Specification developer | 2 | August 5, 1994 | 0 | 0 | 0 | api.fda.gov |
| Endo-Therapeutics, Inc. | Clearwater, FL, United States | Manufacturer | 2 | May 8, 1980 | 0 | 0 | 0 | api.fda.gov |
| Hobbs Medical, Inc. | Stafford Springs, CT, United States | Manufacturer | 2 | January 3, 1985 | 0 | 2 | 0 | api.fda.gov |
| TeleMed Systems | Northborough, MA, United States | Specification developer | 2 | April 2, 2001 | 0 | 1 | 0 | api.fda.gov |
| Cook Incorporated | Bloomington, IN, United States | Complaint file establishment, Manufacturer | 1 | April 11, 1988 | 0 | 0 | 0 | api.fda.gov |
| Cook Incorporated | Spencer, IN, United States | Manufacturer | 1 | April 11, 1988 | 0 | 0 | 0 | api.fda.gov |
| Envision Endoscopy Inc. | Waltham, MA, United States | Complaint file establishment, Manufacturer, Specification developer | 1 | December 20, 2024 | 0 | 0 | 0 | api.fda.gov |
| Stryker Endoscopy | San Jose, CA, United States | Specification developer | 1 | September 10, 1997 | 0 | 0 | 0 | api.fda.gov |
| Slater Endoscopy, LLC | Miramar, FL, United States | Manufacturer | 1 | June 8, 2015 | 0 | 0 | 0 | api.fda.gov |
| United States Endoscopy Group, Inc. | Mentor, OH, United States | Manufacturer | 1 | May 30, 2012 | 0 | 1 | 0 | api.fda.gov |
| Usgi Medical | San Clemente, CA, United States | Manufacturer | 1 | January 14, 2011 | 0 | 0 | 0 | api.fda.gov |
| Atc Technologies Inc. | Wilmington, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ovesco Endoscopy USA | Cary, NC, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Robling Medical, LLC | Youngsville, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.