J. Jamner Surgical Instruments, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 11
- FDA recalls
- 2
At a glance
Market reach
- United States
- FDA recalls
What J. Jamner Surgical Instruments, Inc. makes
The company manufactures reusable surgical instruments and endoscopic tools, including lung forceps, uterine tenaculum forceps, sinus instruments, and aortic punch devices. Their portfolio also covers endoscopes for medical examinations and catalogued surgical instruments for general use.
These products are regulated under FDA 510(k) clearance, with devices classified as Class I or Class II. The company’s instruments are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Search and filter all 11 devicesFDA recalls
2006
- 14 Nov 2006 Z-0596-2007 Unclassified (pre-2012) Terminated The JariTrak Table Clamp may not securely fasten to the bed rail of the OR table during set up of the retractor system. In the event that the clamp is not securely fastened to the bed rail, the system may move during surgery. The firm received several complaints from hospitals.
- 24 Apr 2006 Z-1506-06 Unclassified (pre-2012) Terminated The Ruggles Leyla Ball Joint Clamp may not properly tighten onto the Rigid Holding Rod. Although this condition can be observed during assembly, if the device were to be used during surgery, any attachments to the Rigid Holding Rod could move.
Frequently asked questions
How many devices does J. Jamner Surgical Instruments, Inc. have in the registry?
The registry currently lists 11 devices for J. Jamner Surgical Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list J. Jamner Surgical Instruments, Inc.'s devices?
Among its 11 most recently registered devices, J. Jamner Surgical Instruments, Inc. has devices listed in FDA 510(k) (11 devices).
What risk classes do J. Jamner Surgical Instruments, Inc.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for J. Jamner Surgical Instruments, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for J. Jamner Surgical Instruments, Inc.?
FDA recall records list 2 recalls initiated by J. Jamner Surgical Instruments, Inc., the most recent initiated on 2006-11-14. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from J. Jamner Surgical Instruments, Inc. in the registry?
The most recently registered devices listed for J. Jamner Surgical Instruments, Inc. include JARIT ENDOSCOPES, 600-600; 600-630; 600-650; 680, COPE LUNG FORCEPS #305-218, JARIT SURGICAL INSTRUMENTS and JARIT RECOMMENDED SINUS INSTRUMENTS.