Propper Mfg. Co., Inc.
United Statesfrom the FDA registration address FDA establishment FEI 2410251
- Devices
- 25
- Registrations
- FDA
- FDA recalls
- 2
What Propper Mfg. Co., Inc. makes
Propper Mfg. Co., Inc. makes medical devices such as sterilization indicators, biological and chemical indicators, test packs, laryngoscope blades, and fiber optic scopes including sigmoidoscopes and proctoscopes. Their products include the OK Flash Sterilization Indicator, Bio-Challenge Test Pak, and Propper Super Seracult, among others.
The company's portfolio is regulated under Class I and Class II devices and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Search and filter all 25 devicesCompany details
- FDA FEI number
- 2410251
- Address
- 36-04 SKILLMAN AVE., Long Island City, NY, 11101
FDA recalls
FDA recall records list 2 recalls initiated by PROPPER MFG. CO., INC., the earliest on 2002-08-09 and the most recent on 2008-02-07. By recorded status: 2 terminated. The reasons filed fall into these groups: performance or accuracy and manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2008
- 7 Feb 2008 Z-2330-2008 Unclassified (pre-2012) Terminated The firm discovered a production specification discrepancy that may cause the indicators to show an inaccurate result.
2002
- 9 Aug 2002 Z-0051-04 Unclassified (pre-2012) Terminated Deviation in capillary tubes could cause a 10% increase in read out values which could make a slight anemic patient appear to have a normal reading.
Frequently asked questions
How many devices does PROPPER MFG. CO., INC. have in the registry?
The registry currently lists 25 devices for PROPPER MFG. CO., INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list PROPPER MFG. CO., INC.'s devices?
Among its 25 most recently registered devices, PROPPER MFG. CO., INC. has devices listed in FDA 510(k) (25 devices).
What risk classes do PROPPER MFG. CO., INC.'s devices fall under?
Among its 25 most recently registered devices, the classes recorded for PROPPER MFG. CO., INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for PROPPER MFG. CO., INC.?
FDA recall records list 2 recalls initiated by PROPPER MFG. CO., INC., the most recent initiated on 7 Feb 2008. 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 PROPPER MFG. CO., INC. in the registry?
The most recently registered devices listed for PROPPER MFG. CO., INC. include OK FLASH STERILIZATION INDICATOR, BI-O.K.(TM)-BIOLOGICAL/CHEMICAL INDICATOR, ONCE-A-DAY VERTOS TEST PACK and BIO-CHALLENGE TEST PAK.