Skip to the page

Data / Medical devices / United States / Brymill Corporation

Brymill Corporation: FDA-registered device maker in Ellington, CT, United States, 1 510(k) clearance

Brymill Corporation is registered with the FDA (registration 1216795) in Ellington, CT, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 25, 2020. Registered through 2027. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
1216795
Address
105 Windermere Ave Bldg 2, Ellington, CT, United States, 06029
Owner or operator
BRYMILL CORP. DBA Brymill Cryogenic Systems (1216795)
Roles
Manufacturer
First device listed
May 9, 2023
Registered through
2027
Brand names listed
101 - 310 Cryosurgical Accessories, B-400 Cry-Baby Liquid Nitrogen Cryosurgical System 4 oz., B-501 Liquid Nitrogen Dewar Line, B-700 Cry-Ac Liquid Nitrogen Cryosurgical System 16 oz., B-800 Cry-Ac-3 Liquid Nitrogen Cryosurgical System 10 oz.

Devices it lists

DeviceProduct codeClassRoleSource
Unit, Cryosurgical, AccessoriesGEH2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
March 25, 2020K193619Cry-Ac®, Cry-Ac-3®, Cry-BabyGEHSubstantially EquivalentBrymill Cryogenic Systemsaccessdata.fda.gov

Compare with other makers

Updated March 25, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.