Data / Medical devices / Bangladesh / Shun Ho (bangladesh) Manufactory Limited
Shun Ho (bangladesh) Manufactory Limited: FDA-registered device maker in Cumilla Zilla Chittagong(Division), Bangladesh, 1 510(k) clearance
Shun Ho (bangladesh) Manufactory Limited is registered with the FDA (registration 3009648765) in Cumilla Zilla Chittagong(Division), Bangladesh. It lists 10 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 14, 2011. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3009648765
- Address
- Plot #, Cumilla EPZ, Cumilla Zilla Chittagong(Division), Bangladesh, 3500
- Owner or operator
- Shun Ho (Bangladesh) Manufactory Limited (10040853)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- May 25, 2012
- Registered through
- 2026
- Brand names listed
- 02806MCK2,MCKESSON PREM COMB DOUCHE 12/12, 02814MCK2,MCK F & T WATER BOTTLE 12/12, 02816CV2,CVS WATER BOTTLE 12/12, 02816TC1,TR WATER BOTTLE 12/12, 400570CV2,CVS FINGER SPLINT 2PK (310272) 6/144, 67022,POCKET PILL FOB 6/72, 67054, AM/PM TRAVEL PILL REMINDER 6/72, 67054AMT-120,AM/PM TRAVEL PILL REMINDER (EU) 1/72 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Applicator, Vaginal | HGD | 1 | Contract manufacturer | accessdata.fda.gov |
| Bag, Ice | KYR | 1 | Contract manufacturer | accessdata.fda.gov |
| Bottle, Hot/Cold Water | FPF | 1 | Contract manufacturer | accessdata.fda.gov |
| Case, Contact Lens | LRX | 2 | Manufacturer | accessdata.fda.gov |
| Dispenser, Solid Medication | NXB | 1 | Contract manufacturer | accessdata.fda.gov |
| Douche Apparatus, Vaginal, Therapeutic | HED | 1 | Contract manufacturer | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | Contract manufacturer | accessdata.fda.gov |
| Pad, Eye | HMP | 1 | Manufacturer | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 | Contract manufacturer | accessdata.fda.gov |
| Splint, Hand, And Components | ILH | 1 | Contract manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 14, 2011 | K111856 | SOFT GRIP CONTACT LENS CASE, DELUXE CONTACT LENS CASE, ECONO-MATE CONTACT LENS CASE | LRX | Substantially Equivalent | Apothecary Products, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Bottle, Hot/Cold Water
- All makers of Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
- All makers of Dispenser, Solid Medication
- All makers of Pad, Eye
- All makers of Applicator, Vaginal
- All makers of Case, Contact Lens
Updated July 14, 2011. 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.