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JMA Optic 01570011

by zebris MEDICAL GmbH

JMA Optic 01570011 is a Class I device made by zebris MEDICAL GmbH, listed in FDA GUDID since 1 Mar 2022 (UDI-DI B915015700111), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB915015700111 UDI-DI Date1 Mar 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
JMA Optic
Generic name
Facebow
Model / Ref / Catalog
01570011
Primary DI / UDI-DI
B915015700111
FDA product code
NFS
GMDN term
Facebow
Device class
Class I
Regulation number
872.2060
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Facebow

Similar devices in this category

Other devices filed under Facebow.

Other devices from zebris MEDICAL GmbH

See all devices from zebris MEDICAL GmbH →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)