Planer Plc is one of 19082 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Planer Plc - FDA 510(k) Cleared Devices
Recent clearances: PLANER BT37 INCUBATOR, KRYO ART CONTROLLED RATE FREEZER
2
Total
2
Cleared
0
Denied
Planer Plc, specializes in Obstetrics & Gynecology devices with a manufacturing facility in Pleasant Hill, US. The company develops controlled-rate freezers and incubation systems for reproductive medicine and cryopreservation applications.
Planer Plc has received 2 FDA 510(k) clearances from 2 total submissions. All submissions focused on Obstetrics & Gynecology devices. The company's regulatory activity spans from 2004 to 2012, establishing a historical record in the fertility and cryogenic storage sector.
The company is currently inactive with no FDA 510(k) clearances recorded in the past decade. This profile serves as a historical reference for Planer's contributions to reproductive medicine technology.
FDA 510(k) Regulatory Record - Planer Plc
2 devices