Colgate-Palmolive Company
United Statesfrom the FDA registration address FDA establishment FEI 2221095
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 5
What Colgate-Palmolive Company makes
The company manufactures oral hygiene products, including dental creams, mouthrinses, dental floss, and a periodontal irrigation device for subgingival cleaning. These products are designed for daily dental care, tooth sensitivity relief, and gum health maintenance.
The portfolio includes Class I and Class II devices, with some products authorised via the FDA’s 510(k) pathway. The company is based in the United States and its products are listed in the FDA’s 510(k) registry.
Catalogue
- Registry: GUDID
Periogard(R) Periopen Ref K901955
Regimes: 510(k) Registry: 510(k)Colgate Desensitizing Dental Cream Ref K103461
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Colgate Precision Mint Wzxed Dental Floss Ref K944886
Regimes: 510(k) Registry: 510(k)Colgate Dental Floss Ref K883335
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 2221095
- Address
- 909 RIVER RD, PISCATAWAY, NJ, 08855
FDA recalls
FDA recall records list 5 recalls initiated by Colgate-Palmolive Company, initiated on 2012-03-23. By recorded status: 5 terminated. The reasons filed fall into these groups: electrical or power. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2012
- 23 Mar 2012 Z-1870-2012 Class II Terminated Brush battery cap was forcibly blown off at the end of the brush handle.
- 23 Mar 2012 Z-1871-2012 Class II Terminated Brush battery cap was forcibly blown off at the end of the brush handle.
- 23 Mar 2012 Z-1872-2012 Class II Terminated Brush battery cap was forcibly blown off at the end of the brush handle.
- 23 Mar 2012 Z-1873-2012 Class II Terminated Brush battery cap was forcibly blown off at the end of the brush handle.
- 23 Mar 2012 Z-1874-2012 Class II Terminated Brush battery cap was forcibly blown off at the end of the brush handle.
Frequently asked questions
How many devices does Colgate-Palmolive Company have in the registry?
The registry currently lists 6 devices for Colgate-Palmolive Company. Devices recorded under merged duplicate company entries are counted once.
Which registries list Colgate-Palmolive Company's devices?
Among its 6 most recently registered devices, Colgate-Palmolive Company has devices listed in FDA 510(k) (5 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Colgate-Palmolive Company's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Colgate-Palmolive Company's devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Colgate-Palmolive Company?
FDA recall records list 5 recalls initiated by Colgate-Palmolive Company, the most recent initiated on 23 Mar 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 Colgate-Palmolive Company in the registry?
The most recently registered devices listed for Colgate-Palmolive Company include Colgate Prorelief Sensitivity Relief Serum US05563A, PERIOGARD(R) PERIOPEN, COLGATE DESENSITIZING DENTAL CREAM and COLGATE DESENSITIZING MOUTHRINSE, COLGATE SENSITIVE PRO-RELIEF MOUTHWASH.