Medical Device Manufacturer · US , Walker , MI

Allergan, Inc. - FDA 510(k) Cleared Devices

33 submissions · 33 cleared · Since 1982

Total

Cleared

Denied

Allergan, Inc. was an American global pharmaceutical company headquartered in Walker, US. The company focused on eye care, neurosciences, medical dermatology, and medical aesthetics before ceasing independent operations in 2015.

Allergan received 33 FDA 510(k) clearances from 33 total submissions between 1982 and 2019. The company's regulatory portfolio was dominated by Ophthalmic devices, which accounted for 88% of all submissions. Notable cleared products include the XEN Glaucoma Treatment System, REFRESH rewetting drops, and the Natrelle tissue expander for surgical applications.

Now part of Allergan plc (formerly Actavis), the company's regulatory record reflects its historical significance in eye care innovation and surgical device development. This profile serves as a historical record of the company's FDA 510(k) clearance activity.

Explore the complete list of device names, product codes, and clearance dates in the database.