Data / Medical devices / Taiwan / Peng Lim Enterprise Co., Ltd.
Peng Lim Enterprise Co., Ltd.: FDA-registered device maker in Kaohsiung, Taiwan, 1 510(k) clearance
Peng Lim Enterprise Co., Ltd. is registered with the FDA (registration 8043296) in Kaohsiung, Taiwan. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 14, 2006. Registered through 2026. FDA data exported November 2, 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
- 8043296
- FEI number
- 3008069117
- Address
- No.42, Wanxing Street, Sanmin District, Kaohsiung, Taiwan, 807
- Owner or operator
- PENG LIM ENTERPRISE CO., LTD. (8043296)
- Roles
- Manufacturer
- First device listed
- December 29, 2006
- Registered through
- 2026
- Brand names listed
- DENTAL HANDPIECE, KID CROWN
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Crown, Preformed | ELZ | 1 | Manufacturer | accessdata.fda.gov |
| Handpiece, Air-Powered, Dental | EFB | 1 | 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 |
|---|---|---|---|---|---|---|
| December 14, 2006 | K062947 | HIGH SPEED AIR TURBINE HANDPIECE, MODELS SUPER-AIR AND SUPER-QD SERIES | EFB | Substantially Equivalent | Peng Lim Enterprise Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated December 14, 2006. 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.