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Variant Spo-151-113

by Camber Spine Technologies

Variant Spo-151-113 is a Class I device made by Camber Spine Technologies, listed in FDA GUDID since 25 Nov 2022 (UDI-DI B030SPO1511130), 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 NumberB030SPO1511130 UDI-DI Date25 Nov 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  • Withdrawn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
Variant
Generic name
Ophthalmic surgical device handling forceps, reusable
Model / reference
SPO-151-113
Primary DI / UDI-DI
B030SPO1511130
FDA product code
GAD
GMDN term
Ophthalmic surgical device handling forceps, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Ophthalmic surgical device handling forceps, reusable

Similar devices in this category

Other devices filed under Ophthalmic surgical device handling forceps, reusable.

Other devices from Camber Spine Technologies

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)