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Guide-cap_Drs Light Claver CL0200210

by Good Doctors Co., Ltd.

Guide-cap_Drs Light Claver CL0200210 is a dental/surgical polymerization lamp (FDA Class II; FDA product code EBZ, Activator, Ultraviolet, For Polymerization) made by Good Doctors Co., Ltd., cleared under FDA 510(k) K093751 on 24 Feb 2010 and listed in FDA GUDID since 22 Nov 2019 (UDI-DI 08800025400227), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K093751

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08800025400227 UDI-DI Date22 Nov 2019ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK093751 Date24 Feb 2010DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K093751 decided 24 Feb 2010 Active
  • FDA GUDID UDI-DI 08800025400227 listed 22 Nov 2019 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K093751
  2. Listed FDA GUDID 08800025400227

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Guide-cap_Drs Light Claver
Generic name
Dental/surgical polymerization lamp
Model / reference
CL0200210
Primary DI / UDI-DI
08800025400227
510(k) Number
FDA product code
EBZ
GMDN term
Dental/surgical polymerization lamp
Device class
Class II
Regulation number
872.6070
GUDID distribution status
In Commercial Distribution

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Properties

  • Lot / batch number
Other properties (14, all answered No)