Ssl Americas
Country not established
- Devices
- 16
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Search and filter all 16 devicesFDA recalls
2002
- 25 Nov 2002 Z-0346-03 Unclassified (pre-2012) Terminated Sulfur particles on the surface of gloves.
Full distribution text
- 25 Nov 2002 Z-0346-03 Unclassified (pre-2012) Terminated Sulfur particles on the surface of gloves.
Frequently asked questions
How many devices does Ssl Americas have in the registry?
The registry currently lists 16 devices for Ssl Americas. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ssl Americas's devices?
Among its 16 most recently registered devices, Ssl Americas has devices listed in FDA 510(k) (16 devices).
What risk classes do Ssl Americas's devices fall under?
Among its 16 most recently registered devices, the classes recorded for Ssl Americas's devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Ssl Americas?
FDA recall records list 1 recall initiated by Ssl Americas, the most recent initiated on 25 Nov 2002. 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 Ssl Americas in the registry?
The most recently registered devices listed for Ssl Americas include DUREX MALE COLORED LATEX CONDOMS WITH SCENTED LUBRICANTS, DUREX SPEARMINT SCENTED LUBRICATED LATEX CONDOM (DUREX 'TINGLING PLEASURE' CONDOM, DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT and DUREX PLAY SOFT & SENSUAL LUBRICANT.