Avalign VM91-0126
Avalign VM91-0126 is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 1 May 2017 (UDI-DI 00190776032814), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00190776032814 | Date1 May 2017 | StatusListed |
Official records
- AccessGUDID record 00190776032814
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Avalign
- Generic name
- Bench-top keratometer
- Model / reference
- VM91-0126
- Primary DI / UDI-DI
- 00190776032814
- FDA product code
- HOE
- GMDN term
- Bench-top keratometer
- Device class
- Class I
- Regulation number
- 886.4350
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices
Other devices filed under FDA product code HOE (Caliper, ophthalmic).
- Oph. Caliper 08-12101 by Katena Products, Inc.
- CALIPER-OPTHALMIC by Design Research Assoc., Inc.
- Ophthalmic Caliper K3-9030 by Katena Products, Inc.
- BLEPHAROMETER by Aztec Medical Products, Inc.
- Stephens Instruments S4-1458 by KRISHNA IMPORTS INC
- KOI(TM) BLADE GAUGE, MODEL KOI-132 by COOPERVISION INC.
- Stephens Instruments S4-1457 by KRISHNA IMPORTS INC
- BLADE GAUGE by Koi, Inc.
- KELMAN DIPSTICK by V. Mueller O.V. Baxter Healthcare Corp.
- KREMER BLADE GAUGE by ACCUTOME, INC.