Data / Medical devices / China / Tiger Medical Group
Tiger Medical Group: FDA-registered device maker in Shanghai, China, 3 510(k) clearances
Tiger Medical Group is registered with the FDA (registration 3004488394) in Shanghai, China. It lists 38 device types. The FDA files 3 510(k) clearances under its listings, the newest dated January 26, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004488394
- Address
- Jaje Plaza, Suite North Sichuan Road, Shanghai, China, 200080
- Owner or operator
- ASP Tiger, LLc (9055664)
- Roles
- Exporter to the US, Repackager or relabeler, Specification developer
- First device listed
- August 23, 2006
- Registered through
- 2026
- Brand names listed
- Cap various, multiple, Casting bandage, Casting tape, Catheter and Tip, Yankauer, Suction; Multiple, Various, DISP. OROPHARYNGEAL AIRWAYS, MULT., EMESIS BAGS, FILM DRESSING, Isolation gown and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Specification developer | accessdata.fda.gov |
| Aid, Transfer | IKX | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Airway, Oropharyngeal, Anesthesiology | CAE | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Applicator, Absorbent Tipped, Sterile | KXG | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Bandage, Cast | ITG | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Bandage, Elastic | FQM | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Basin, Emesis | FNY | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Blood Pressure Cuff | DXQ | 2 | Exporter to the US | accessdata.fda.gov |
| Cannula, Nasal, Oxygen | CAT | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Cap, Surgical | FYF | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Catheter And Tip, Suction | JOL | 2 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Catheters, Suction, Tracheobronchial | BSY | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use | JQC | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Container, Specimen, Non-Sterile | NNI | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Container, Specimen, Sterile | FMH | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Cover, Limb | IPM | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Coverslips, Microscope Slide | KES | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Crutch | IPR | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use | LXG | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Infusor, Pressure, For I.V. Bags | KZD | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Mask, Oxygen | BYG | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Mask, Oxygen, Non-Rebreathing | KGB | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Non-Surgical Gown | OEA | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Orthosis, Lumbar | IQE | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Patient Personal Hygiene Kit | NSB | 1 | Exporter to the US, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Razor, Surgical | LWK | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Set, Tubing And Support, Ventilator (W Harness) | BZO | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Shoe And Shoe Cover, Conductive | BWP | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Slides, Microscope | KEW | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Speculum, Vaginal, Nonmetal | HIB | 2 | Exporter to the US | accessdata.fda.gov |
| Staple, Removable (Skin) | GDT | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Stethoscope, Manual | LDE | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Toothbrush, Manual | EFW | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Tourniquet, Nonpneumatic | GAX | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Walker, Mechanical | ITJ | 1 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Wrap, Sterilization | FRG | 2 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| January 26, 2011 | K102792 | DISPOSABLE BLOOD PRESSURE CUF | DXQ | Substantially Equivalent | Caremate Medical Device Co., Ltd. | accessdata.fda.gov |
| December 27, 2007 | K071886 | SELF SEAL STERILIZATION POUCH | FRG | Substantially Equivalent | Shanghai Jianzhong Medical Packaging Co., Ltd. | accessdata.fda.gov |
| July 11, 2005 | K050887 | GONGDONG DISPOSABLE VAGINAL SPECULUM | HIB | Substantially Equivalent | Zhejiang Gongdong Medical Plastic Factory | accessdata.fda.gov |
Compare with other makers
- All makers of Tape And Bandage, Adhesive
- All makers of Tourniquet, Nonpneumatic
- All makers of Gauze / Sponge,Nonresorbable For External Use
- All makers of Container, Specimen, Non-Sterile
- All makers of Toothbrush, Manual
- All makers of Stethoscope, Manual
Updated January 26, 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.