Activator 3000-0017
Activator 3000-0017 is a Class I device made by Allesee Aoa-Pro, listed in FDA GUDID since 13 Mar 2023 (UDI-DI 00889989038507), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00889989038507 | Date13 Mar 2023 | StatusListed |
Official records
- AccessGUDID record 00889989038507
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Activator
- Generic name
- Orthodontic palate expander/teeth aligner, self-removable
- Model / reference
- 3000-0017
- Primary DI / UDI-DI
- 00889989038507
- FDA product code
- KMY
- GMDN term
- Orthodontic palate expander/teeth aligner, self-removable
- Device class
- Class I
- Regulation number
- 872.5525
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code KMY (POSITIONER, TOOTH, PREFORMED).
- KeyPrint 4220155 by Keystone Industries
- Proform 9614830R2 by Keystone Industries
- GLENROE ELASTIBITE STIMULATOR by Glenroe Technologies
- PERFORMED TEMPLATE W/FRAGRANCE FOR TOOTH POSTIONER by American Orthodontics
- RELAX-O-GUARD by Aquatemp Service Co., Inc.
- AQUALIZER MOUTHPIECE by Martin D. Lerman
- DYNAMIC FUNTIONAL POSITIONER by Dynamic Functional Positioner, Inc.
- DENT-O-CRYL ORTHODONTIC ACRYLIC by Dentauraum, Inc.
- PREFORMED TOOTH POSITIONER by Tp Laboratories, Inc.
- REMOLDABLE CRANIOMANDIBULAR APPLIANCE by Jeffrey H. Attlin