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Pharmacia & Upjohn Co.

US

Last updated May 23, 2026

What Pharmacia & Upjohn Co. makes

Pharmacia & Upjohn Co. makes collagen haemostatic agents such as Gelfoam and Gelfilm, surgical anti-adhesion materials, medicated and non-medicated surgical procedure kits, cervical dilatation catheters, vaginal applicators (both single-use and reusable), and empty self-injectors including the Genotropin Pen® 5.

The company's devices are classified as Class I, II, and III and are listed in the FDA 510(k) and FDA UDI registries. Pharmacia & Upjohn Co. is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Pharmacia & Upjohn Co. manufacture?

Pharmacia & Upjohn Co. manufactures collagen haemostatic agents like Gelfoam and Gelfilm, surgical anti-adhesion materials that are implantable and bioabsorbable, medicated and non-medicated surgical procedure kits (including single-use versions), cervical dilatation catheters, vaginal applicators (both single-use and reusable), and empty self-injectors such as the Genotropin Pen® 5. These products are derived directly from the device categories and example devices provided in the data.

Where is Pharmacia & Upjohn Co. based?

Pharmacia & Upjohn Co. is based in the United States, as explicitly stated in the SUMMARY section of the device data. The COUNTRY field also confirms this as US, indicating the company’s headquarters or primary operational location is within the United States.

In which regulatory registries are Pharmacia & Upjohn Co.'s devices listed?

Pharmacia & Upjohn Co.'s devices are listed in the FDA 510(k) and FDA UDI registries, as specified in the LISTED IN field of the device data. These registries track devices that have undergone premarket notification or require unique device identification for traceability, but listing does not imply approval of the company itself.

How are Pharmacia & Upjohn Co.'s devices classified by regulatory risk?

Pharmacia & Upjohn Co.'s devices are classified as Class I, Class II, and Class III, according to the DEVICE CLASSES field in the data. This range indicates the company produces devices across low to high risk categories, with Class III representing the highest level of regulatory scrutiny due to factors like implantability or life-sustaining function.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
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Catalogue (38)

DeviceModel / ReferenceRegistriesClassStatus
CLEOCIN® (clindamycin phosphate vaginal cream, USP), 7 day NDC 0009-3448-01
FDA UDI
Class IActive
Gelfoam Size 100 - Compressed
FDA UDI
Class IIIActive
Gelfilm Gelfilm® Sterile Ophthalmic Film Ophthalmic film 6's (12.5 sq cm)
FDA UDI
Class IIActive
Clindamycin phosphate vaginal cream, USP, 7 day (Greenstone) NDC 59762-5009-1
FDA UDI
Class IActive
Gelfoam 1 g Powder
FDA UDI
Class IIIActive
Gelfoam Size 50
FDA UDI
Class IIIActive
CLEOCIN® (clindamycin phosphate vaginal suppositories) Vaginal Ovules NDC 0009-7667-01
FDA UDI
Class IActive
Gelfoam Size 4, 2 sponges per envelope
FDA UDI
Class IIIActive
GELFOAM-JMI™ Sponge Kit Size 100
FDA UDI
Class IIIActive
Genotropin Pen® 5 F000116153
FDA UDI
Class IIActive
Gelfoam Size 200
FDA UDI
Class IIIActive
GELFOAM-JMI™ Powder Kit 1 g Powder
FDA UDI
Class IIIActive
Gelfoam Size 100
FDA UDI
Class IIIActive
Gel-Flow™ Nt Hemostatic Matrix for Flowable Applications - 6 mL
FDA UDI
Class IIIActive
Gelfilm Gelfilm® Sterile Film Sterile film 1's (125 sq cm)
FDA UDI
Class IIActive
Gelfoam Size 12-7
FDA UDI
Class IIIActive
Prepidil® Gel, dinoprostone cervical gel NDC 0009-3359-01
FDA UDI
N/AActive
Gel-Flow Kit 6 mL
FDA UDI
Class IIIActive
Gelfilm Gelfilm® Sterile Film Sterile film 1's (125 sq cm)
FDA UDI
Class IIUnknown
Genotropin Pen® 12 F000099111
FDA UDI
Class IIActive
Varelisa Rnp Antibodies K993589
FDA 510(k)
Class IIActive
Unicap Thyroid Peroxidase Igg K981930
FDA 510(k)
Class IIActive
Allergen Immundocap Modelc5, C6, C73, E201, E213, F50, F51, F54, F55, F56, F57, F58, F59, F60, F61, F205, F213, F218, F K993388
FDA 510(k)
Class IIActive
Unicap Gliadin Iga Assay K982533
FDA 510(k)
Class IIActive
Unicap Gliadin Igg Assay K982701
FDA 510(k)
Class IIActive
Pharmacia Cap System Ige Feia, Model 10-9395-01 K991945
FDA 510(k)
Class IIActive
Unicap Thyroglobulin Igg Assay, Unicap Thyroid Peroxidase Igg Assay K981559
FDA 510(k)
Class IIActive
Varelisa Sm Antibodies K000312
FDA 510(k)
Class IIActive
Allergen Immunocap, Models C74, E89, Ex2, Ex70, Ex71, Ex73, Fx8, Fx9, Fx10, Fx16, Fx73, I72, I75, I76, K71, K73, K81, K8 K000132
FDA 510(k)
Class IIActive
Varelisa Recombi Ana Screen Eia, Models 128 48/ 128 96 K993108
FDA 510(k)
Class IIActive
Allergen Immunocap F256, F245, F207, F202 K974580
FDA 510(k)
Class IIActive
Allergen Immunocap, Models E7, F93, F94, F95, F203, F204, F208, F209, F210, F214, F216, F235, F237, F242, F255, F259, F2 K991048
FDA 510(k)
Class IIActive
Ceeon Easysert Intraocular Lens Injector, Model Imp-1 K002556
FDA 510(k)
Class IActive
Varelisa Tg (thyroglobulin) Antibodies, K003414
FDA 510(k)
Class IIActive
Pharmacia Cap System Rast Feia K962976
FDA 510(k)
Class IIActive
Allergen Immunocap Models D73, D74, E71, E72, E73, E74 E75, E76, E82, E88, F48, F90, F92, F96, F201, F215, M70, T17, T72, 3 K982343
FDA 510(k)
Class IIActive
Varelisa Tpo Antibodies, Model 12348/12396 K993585
FDA 510(k)
Class IIActive
Varelisa Recombi Ana Profile K993109
FDA 510(k)
Class IIActive

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