Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009648765

FEI Number

3009648765

Entity Name

SHUN HO (BANGLADESH) MANUFACTORY LIMITED

City/State/Country

Cumilla Zilla Chittagong (Division), BD

Establishment Address

Plot # 218-219, Cumilla EPZ, Cumilla Zilla Chittagong (Division) 3500, BD

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Shun Ho (Bangladesh) Manufactory Limited (Owner Number: 10040853)

Owner / Operator Contact Address

Plot # 218-219, Cumilla EPZ, Cumilla Zilla, BD-NOTA 3500, BD

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

67471AB-100,AMZ BSC CARE WKLY AM/PM PP (B0BFRX46G9) BK/NT 1/72 67571HSP-C, HS PB NONLOCKING XL PURPLE 262 - BD 67054, AM/PM TRAVEL PILL REMINDER 6/72 67585, WKLY AM/PM PILL PLNR 6/36 70084, STAINLESS LOCKING CONTAINER 3/24 67571HSR-B, HS PB NONLOCKING XL RED 207 - BD 67571HSB-C, HS PB NONLOCKING XL BLUE 2925 - BD 67571, WKLY PUSH BUTTON PILL PLNR XL 6/72 67583, PUSH BUTTON MEDTIME PLANNER 3/36 80189HS1-A, HS PUSH BUTTON MEDTIME PLNR - BD 67585HS-A, HS PUSH BUTTON AM/PM 7DAY - BD 67585AMZ AM/PM 7 DAY PUSH BUTTON 1/36 67054AMZ AM/PM TRAVEL PILL REMINDER 1/72 67571AMZ PUSH BUTTON NONLOCKING XL 1/72 67583AMZ WG PB MEDTIME PLANNER 36/36 67022,POCKET PILL FOB 6/72 68130,DELUXE METAL PILL FOB 6/72 68130RA2,RITE AID DELUXE METAL PILL FOB 72/72 67284WG5,WG COLOR PILL FOB DSP 12/288 70440AMT1,WKLY AM/PM PILL PLNR RD/BL 1/40 70063MJ2,MEIJER EXTRA LARGE PILL FOB 6/72 67471AMT1,WKLY AM/PM PILL PLNR (EU) 1/72 70063,EXTRA LARGE PILL FOB 6/72 67571TG6 TG Push Button 7 Day 67585WM1,EQ AM/PM WEEKLY LG PB PILL PLANNER 3/24 67471AB-110,AMZ BSC CARE WKLY AM/PM PP (B0BFRTM2R5) BL/NT 1/72 67471CV3,CVS WLY AM/PM PILL PLNR 72/72 68130HB,HEB DELUXE METAL PILL FOB 6/72 67278, COLORED DELUXE PILL FOB 12/288 67284CV5,CVS PILL CADDY 12/288 67471A,WKLY AM/PM PILL PLNR 6/72 68130TC1,TC DELUXE PILL FOB 6/72 Therapeutic Vaginal Douche Aparatus Vaginal Applicator Ice Bag Hot/Cold Water Bottle 97451WM1,EQ FINGER SPLINT 6/72 400570CV2,CVS FINGER SPLINT 2PK (310272) 6/144 70222CV1,CVS DELUXE FINGER SPLINTS BLACK 6/72 97476WG5,WG BASEBALL SPLINT 72/72 70273KG1,KG OPP CONTACT CASE 3CT 12/24 68092CV3,CVS VALUE CONTACT LENS CASE 2CT 36/36 C283TC1,TR EYE CARE CONTACT LENS CASE 6/36 68012A,SLIM LINE SOFT GRIP LENS CASE 3/24 68090A,OPP CONTACT CASE 1CT 6/36 68013A,SOFT GRIP LENS CASE 6/36 68048CV3,CVS COVERLETS CONTACT LENS CASES 4CT 36/36 Opthalamic Eye Shield F414-505WM1,EQUATE CONTOUR EYE PATCH 3/24 Eye mask with gel pad

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HMP	Pad, Eye	General, Plastic Surgery	Class 1	878.4440	2015-06-01
NXB	Dispenser, Solid Medication	Physical Medicine	Class 1	890.5050	2019-05-15
HED	Douche Apparatus, Vaginal, Therapeutic	Obstetrics/Gynecology	Class 1	884.5900	2012-05-25
HGD	Applicator, Vaginal	Obstetrics/Gynecology	Class 1	884.4520	2012-05-25
KYR	Bag, Ice	General Hospital	Class 1	880.6050	2012-05-25
FPF	Bottle, Hot/Cold Water	General Hospital	Class 1	880.6085	2012-05-25
ILH	Splint, Hand, And Components	Physical Medicine	Class 1	890.3475	2025-04-07
LRX	Case, Contact Lens	Ophthalmic	Class 2	886.5928	2025-06-23
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2012-05-25
IME	Pack, Hot Or Cold, Reusable	Physical Medicine	Class 1	890.5700	2015-06-11

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Shun Ho (Bangladesh) Manufactory Limited

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
K944481	Garan Scientific, Inc.	THE HEART PROTECTOR	1995-04-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009648765. Last updated year: 2026. Please use registration number 3009648765 when referencing this establishment in official correspondence.