GEORGE TIEMANN & CO.

FDA registration: United States Last updated 25 Oct 2026

Devices: 1,708
Registries: GUDIDFDA
FDA recalls: 0

Catalogue1,708

Page 4 of 35

Showing 151-200 of 1,708

What GEORGE TIEMANN & CO. makes

GEORGE TIEMANN & CO. makes medical devices such as titanium bone screws.

The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

FDA registration: United States(from the FDA establishment record (FEI))
Address: 25 PLANT AVE., HAUPPAUGE, NY, 11788
FDA FEI number: 2424531

Catalogue1,708

N/A 1057893 Ref 1057893

N/A 030668 Ref 030668

N/A B58210510220 Ref B58210510220

N/A 1051107 Ref 1051107

N/A 1057576 Ref 1057576

N/A B5821609100 Ref B5821609100

N/A B5820309280 Ref B5820309280

N/A 0801780SMB Ref 0801780SMB

N/A 36580 Ref 36580

N/A 065705 Ref 065705

N/A 1051235 Ref 1051235

N/A 126HHP12 Ref 126HHP12

N/A 08082214 Ref 08082214

N/A 10578930 Ref 10578930

N/A 363865 Ref 363865

N/A 0807013 Ref 0807013

N/A B5820301550 Ref B5820301550

N/A 08070111 Ref 08070111

N/A B5821052361F0 Ref B5821052361F0

N/A 105650 Ref 105650

N/A 16055NM Ref 16055NM

N/A 105306 Ref 105306

N/A 361357 Ref 361357

N/A 10560 Ref 10560

N/A 08082312 Ref 08082312

N/A 080HSS GRAFT7 Ref 080HSS GRAFT7

N/A 8085558 Ref 8085558

N/A 105203 Ref 105203

N/A 36437 Ref 36437

N/A 080841X14 Ref 080841X14

N/A 1057205 Ref 1057205

N/A 126HHP09 Ref 126HHP09

N/A 105234 Ref 105234

N/A 030704 Ref 030704

N/A 105567SC Ref 105567SC

N/A 355727 Ref 355727

N/A 1057221 Ref 1057221

N/A 160561 Ref 160561

N/A 803160 Ref 803160

N/A 1051165 Ref 1051165

N/A 105404 Ref 105404

N/A 16054B Ref 16054B

N/A 8029395 Ref 8029395

N/A 0101817 Ref 0101817

N/A 80143540 Ref 80143540

N/A 0807021 Ref 0807021

N/A 803056 Ref 803056

N/A 301285 Ref 301285

N/A 30347 Ref 30347

N/A 800993 Ref 800993

What GEORGE TIEMANN & CO. makes

Information