Data / Medical devices / United States / Health Body World Supply, Inc. Dba The Wabbo Company
Health Body World Supply, Inc. Dba The Wabbo Company: FDA-registered device maker in Lake Elsinore, CA, United States, 4 510(k) clearances
Health Body World Supply, Inc. Dba The Wabbo Company is registered with the FDA (registration 2087190) in Lake Elsinore, CA, United States. It lists 7 device types. The FDA files 4 510(k) clearances under its listings, the newest dated November 13, 2002. Registered through 2026. FDA data exported November 3, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 2087190
- FEI number
- 3003328262
- Address
- 670 W Minthorn Street, Lake Elsinore, CA, United States, 92530
- Owner or operator
- HEALTH BODY WORLD SUPPLY INC DBA THE WABBO COMPANY (9045485)
- Roles
- Specification developer
- First device listed
- October 9, 2007
- Registered through
- 2026
- Brand names listed
- A.POINT, A1, ACUPUNCTURE NEEDLES, CAM, LEGEND, CQ, CQG, E5, ELEMENT CUPPING SET, Element and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adhesive Backed Thermal Skin Patches | OMW | 1 | Specification developer | accessdata.fda.gov |
| Bedding, Disposable, Medical | KME | 1 | Specification developer | accessdata.fda.gov |
| Device, Pressure Applying | KNM | 1 | Specification developer | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Specification developer | accessdata.fda.gov |
| Needle, Acupuncture, Single Use | MQX | 2 | Specification developer | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | Specification developer | accessdata.fda.gov |
| Unit, Heating, Powered | IRQ | 1 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| November 13, 2002 | K023054 | JIA CHEN ACUPUNCTURE NEEDLE, FOR SINGLE USE | MQX | Substantially Equivalent | Mandala Health Care, LLC | accessdata.fda.gov |
| September 23, 2002 | K020851 | TDP HEAT LAMP OR INFRARED HEATING LAMP, MODELS CQG-S1, CQG-111A/B, CQG-222A/B, CQG-270A/B, CQG-222D | ILY | Substantially Equivalent | C&H International | accessdata.fda.gov |
| July 9, 2001 | K011669 | BW ACUPUNCTURE NEEDLES | MQX | Substantially Equivalent | H F Intl. Co. | accessdata.fda.gov |
| May 29, 1997 | K964861 | ACUPUNCTURE NEEDLES | MQX | Substantially Equivalent | C.A.M. Supply, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Needle, Acupuncture, Single Use
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Device, Pressure Applying
- All makers of Unit, Heating, Powered
- All makers of Bedding, Disposable, Medical
- All makers of Adhesive Backed Thermal Skin Patches
Updated November 13, 2002. 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.