Midmark LT-1600-102
Midmark LT-1600-102 is a Class I device made by Midmark Corporation, listed in FDA GUDID since 10 Mar 2026 (UDI-DI 00841709122071), 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 | Number00841709122071 | Date10 Mar 2026 | StatusListed |
Official records
- AccessGUDID record 00841709122071
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Midmark
- Generic name
- LED dental light, line-powered
- Model / Ref / Catalog
- LT-1600-102
- Primary DI / UDI-DI
- 00841709122071
- FDA product code
- EAZ
- GMDN term
- LED dental light, line-powered
- Device class
- Class I
- Regulation number
- 872.4630
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Similar devices
Other devices filed under FDA product code EAZ (LIGHT, OPERATING, DENTAL).
- Maintenance Kit AIL0206 by ZYRIS, INC.
- LUVIS-C200 Series C200-C0S1A0 by DENTIS CO., LTD
- COXO CX249-23 by Foshan COXO Medical Instrument Co., Ltd.
- DENTAL EQUIPMENT PROTECTION DEVICES by Pro-Safe Professional Linens, Inc.
- RITTER STARLIGHT DENTAL OPERATING LIGHT by Ritter Co.
- LUVIS-C700 Series C700-W0S0A0 by DENTIS CO., LTD
- KLIP-LITE by Innovators, Inc.
- Maintenance Kit AIL0239 by ZYRIS, INC.
- DELIGHT by Planmeca USA, Inc.
- Ceiling Modell 6571272 by SIRONA Dental Systems GmbH