Lakewood Ent., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Lakewood Ent., Ltd. makes
Lakewood Ent., Ltd. manufactures latex examination gloves, designed for medical and clinical use to ensure barrier protection during patient examinations and procedures.
These products are classified as Class I devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Latex Examination Gloves Ref K893304
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lakewood Ent., Ltd. have in the registry?
The registry currently lists 1 device for Lakewood Ent., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lakewood Ent., Ltd.'s devices?
Among its 1 most recently registered device, Lakewood Ent., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Lakewood Ent., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lakewood Ent., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Lakewood Ent., Ltd. in the registry?
The most recently registered devices listed for Lakewood Ent., Ltd. include LATEX EXAMINATION GLOVES.