Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009191551

FEI Number

3009191551

Entity Name

SAGE SERVICES GROUP

City/State/Country

Charleston, SC, US

Establishment Address

506 Deanna Ln, Charleston, SC 29492, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Sage Services Group (Owner Number: 10039289)

Owner / Operator Contact Address

506 Deanna lane, Charleston, SC 29492, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K112544

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DSA	Cable, Transducer And Electrode, Patient, (Including Connector)	Cardiovascular	Class 2	870.2900	2016-04-21
DXQ	Blood Pressure Cuff	Cardiovascular	Class 2	870.1120	2016-04-21
DQA	Oximeter	Cardiovascular	Class 2	870.2700	2016-04-21
DSA	Cable, Transducer And Electrode, Patient, (Including Connector)	Cardiovascular	Class 2	870.2900	2016-04-21
FLL	Continuous Measurement Thermometer	General Hospital	Class 2	880.2910	2016-04-21
DXQ	Blood Pressure Cuff	Cardiovascular	Class 2	870.1120	2016-04-21

Official Correspondent

Joe Harper

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sage Services Group

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
K880323	Medtronic Vascular	MEDTRONIC MODEL 5411 SURGICAL CABLE ADAPTOR	1988-03-22
K831001	Frontier Products	UNICUFF-BLOOD PRESSURE CUFF	1983-07-28
K253089	Shenzhen Best Electronics Co., Ltd.	NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722)	2026-02-13
K972301	Rudolf Riester GmbH & Co. KG	BIG BEN SQUARE, BIG BEN ROUND	1997-09-17
K903523	Hewlett-Packard Co.	HP MODEL M1020A, ARTERIAL OXYGEN SAT/PLETH MODULE	1990-10-23

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0020-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	CAPNOSTREAM 20 (US) N, Part Number CS08651
Z-0022-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-02
Z-0023-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-03
Z-0028-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	Capnostream20 (US) M, Part Number CS08653
Z-0029-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	Capnostream20 (US) M W/PRINTER, Part Number CS08659

Similar Registrations

Registration Number	Establishment Name	Location
3017528618	ATRILITY MEDICAL, INC.	Madison, WI, US
3017619000	SHENZHEN REDY-MED TECHNOLOGY CO., LTD.	Shenzhen Guangdong, CN
2939520	VOLCANO CORPORATION	Rancho Cordova, CA, US
3017636737	STERIS Corporation de Republica Dominicana, S.R.L.	Santo Domingo, DO
3004859241	BOSTON SCIENTIFIC CORPORATION	La Aurora Heredia, CR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009191551. Last updated year: 2026. Please use registration number 3009191551 when referencing this establishment in official correspondence.