Wave Form Mfg., Inc.
Country not established
- Devices
- 1
What Wave Form Mfg., Inc. makes
Wave Form Mfg., Inc. manufactures prolase general shaped fiber, a medical device designed for surgical or clinical applications requiring absorbable, shaped fiber materials.
The company’s products are classified as Class II under FDA regulations and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wave Form Mfg., Inc. have in the registry?
The registry currently lists 1 device for Wave Form Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wave Form Mfg., Inc.'s devices?
Among its 1 most recently registered device, Wave Form Mfg., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Wave Form Mfg., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wave Form Mfg., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wave Form Mfg., Inc. in the registry?
The most recently registered devices listed for Wave Form Mfg., Inc. include WAVE FORM MANUFACTURING PROLASE GENERAL SHAPED FIBER.