BRYMILL CORPORATION

FDA Device Registration & Listing · ELLINGTON, CT, US · Registration 1216795

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1216795
FEI Number
1216795
Entity Name
BRYMILL CORPORATION
City/State/Country
ELLINGTON, CT, US
Establishment Address
105 Windermere Ave Bldg 2, ELLINGTON, CT 06029, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
BRYMILL CORP. DBA Brymill Cryogenic Systems (Owner Number: 1216795)
Owner / Operator Contact Address
105 WINDERMERE AVE., BLDG. 2, Ellington, CT 06029, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

B-700 Cry-Ac Liquid Nitrogen Cryosurgical System 16 oz. B-400 Cry-Baby Liquid Nitrogen Cryosurgical System 4 oz. B-800 Cry-Ac-3 Liquid Nitrogen Cryosurgical System 10 oz. 101 - 310 Cryosurgical Accessories B-501 Liquid Nitrogen Dewar Line

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GEH Unit, Cryosurgical, Accessories General, Plastic Surgery Class 2 878.4350 2023-05-09

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BRYMILL CORP. DBA Brymill Cryogenic Systems
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K190651 Erbe Elektromedizin GmbH ERBECRYO 2 Cryosurgical Unit; ERBECRYO 2 1-pedal footswitch, Extension cable f. ERBECRYO 2 footswitch; Flexible Cryoprobe; ERBECRYO 2 Cart, VIO-Cart, Wire basket; Connecting hoses, switching valves, adapter 2020-01-07
K760953 Spembly Medical , Ltd. DEEP FREEZE SYSTEM (DFS-30) 1976-11-16

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1216795. Last updated year: 2026. Please use registration number 1216795 when referencing this establishment in official correspondence.
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