Surgical Instruments Service and Savings, Inc.
United StatesFDA applicant, unverified
- Devices
- 31
- FDA recalls
- 22
At a glance
Market reach
- United States
- FDA recalls
What Surgical Instruments Service and Savings, Inc. makes
The company reprocesses single-use surgical instruments, including ultrasonic tools, arthroscopic shapers, electrosurgical devices and accessories, biopsy forceps, phacoemulsification tips, trocars, cannulas, and compression limb sleeves. These items are designed for reuse in laparoscopic, endoscopic, and general surgical procedures.
The portfolio includes devices classified as Class II and Unclassified (U) under FDA regulations, with submissions recorded in the FDA 510(k) registry. The company operates from the United States.
Catalogue
Search and filter all 31 devicesFDA recalls
2013
- 3 May 2013 Z-1623-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1624-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1625-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1626-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1627-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1628-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1629-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1630-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1631-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1632-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
Show all 22 recalls
2013
- 3 May 2013 Z-1633-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1634-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1635-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1636-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1637-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1638-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1639-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1640-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1641-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1642-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1643-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
- 3 May 2013 Z-1644-2013 Class II Terminated The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
Frequently asked questions
How many devices does Surgical Instruments Service and Savings, Inc. have in the registry?
The registry currently lists 31 devices for Surgical Instruments Service and Savings, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgical Instruments Service and Savings, Inc.'s devices?
Among its 31 most recently registered devices, Surgical Instruments Service and Savings, Inc. has devices listed in FDA 510(k) (31 devices).
What risk classes do Surgical Instruments Service and Savings, Inc.'s devices fall under?
Among its 31 most recently registered devices, the classes recorded for Surgical Instruments Service and Savings, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Surgical Instruments Service and Savings, Inc.?
FDA recall records list 22 recalls initiated by Surgical Instruments Service and Savings, Inc., the most recent initiated on 3 May 2013. 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 Surgical Instruments Service and Savings, Inc. in the registry?
The most recently registered devices listed for Surgical Instruments Service and Savings, Inc. include Medline ReNewal Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter (8F, 8FG, 10F, 10FG), Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector, Medline ReNewal Reprocessed ArthroCare ArthroWands and Smith & Nephew Dyonics and Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019).