Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9021987

FEI Number

3000204334

Entity Name

Beekley Corporation

City/State/Country

Bristol, CT, US

Establishment Address

1 PRESTIGE LN, Bristol, CT 06010, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Beekley Corporation (Owner Number: 10023165)

Owner / Operator Contact Address

One Prestige Lane, Bristol, CT 06010, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

AccuGrid CoreTainer SPOTs Localizers PinPoint Altus GuideLines Bella Blankets InkRight ColdSPOT MarginMap CaraClip PointGuards Cradles TenderTouch Pinnacle

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNI	Container, Specimen, Non-Sterile	Pathology	Class 1	864.3250	2008-04-09
JAC	System, X-Ray, Film Marking, Radiographic	Radiology	Class 1	892.1640	2008-04-09
IXJ	Grid, Radiographic	Radiology	Class 1	892.1910	2007-11-07
IZH	System, X-Ray, Mammographic	Radiology	Class 2	892.1710	2008-04-14
FZZ	Marker, Skin	General, Plastic Surgery	Class 1	878.4660	2024-09-17
IMD	Pack, Hot Or Cold, Disposable	Physical Medicine	Class 1	890.5710	2008-04-09
MJI	Specimen/Tissue, Identification Orientation	Pathology	Class 1	864.3010	2008-04-09
MDM	Instrument, Manual, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2023-10-25
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2008-04-09

Official Correspondent

Kate Chase

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Beekley Corporation

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
K880871	John Wagner Associates, Inc.	GRABBER WARM PACK/MINI MINI HEATER/FOOT HEATER	1988-05-20
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29
K870091	Avery Intl.	IV SECUREMENT DEVICE USING PCCE THERMO. FILM	1987-02-04

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0505-2022	Philips North America Llc	1	Infa-Therm Transport Mattress, Reference Number 989805616831 1015
Z-0506-2022	Philips North America Llc	1	Infant Heel Warmers w/strap, Reference # 989805603201 1223

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3017771197	ZARAPAK SDN. BHD.	Perak, MY
3016648678	INNOVERO, LLC	Colorado Springs, CO, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9021987. Last updated year: 2026. Please use registration number 9021987 when referencing this establishment in official correspondence.