Superstat Corp.
Country not established
- Devices
- 1
- FDA recalls
- 13
At a glance
Market reach
- United States
- FDA recalls
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Superstat Ref P810040
Regimes: PMA Registry: PMA
FDA recalls
2012
- 24 Oct 2012 Z-0331-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Full distribution text
- 24 Oct 2012 Z-0332-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Full distribution text
- 24 Oct 2012 Z-0333-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Full distribution text
- 24 Oct 2012 Z-0334-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Full distribution text
- 24 Oct 2012 Z-0335-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Full distribution text
- 24 Oct 2012 Z-0336-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Full distribution text
- 24 Oct 2012 Z-0337-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Full distribution text
- 24 Oct 2012 Z-0338-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Full distribution text
- 24 Oct 2012 Z-0339-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Full distribution text
- 24 Oct 2012 Z-0340-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Full distribution text
- 24 Oct 2012 Z-0331-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Show all 13 recalls
2012
- 24 Oct 2012 Z-0341-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Full distribution text
- 24 Oct 2012 Z-0342-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Full distribution text
- 24 Oct 2012 Z-0343-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Full distribution text
- 24 Oct 2012 Z-0341-2013 Class II Terminated The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Frequently asked questions
How many devices does Superstat Corp. have in the registry?
The registry currently lists 1 device for Superstat Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Superstat Corp.'s devices?
Among its 1 most recently registered device, Superstat Corp. has devices listed in FDA PMA (1 device).
What risk classes do Superstat Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Superstat Corp.'s devices are Class III. Each device page shows its own class and authorisation.
Are there FDA recall records for Superstat Corp.?
FDA recall records list 13 recalls initiated by Superstat Corp., the most recent initiated on 24 Oct 2012. 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 Superstat Corp. in the registry?
The most recently registered devices listed for Superstat Corp. include SUPERSTAT.